| Sl.No |
Mutation type |
Genomic level change |
CDS level change |
RNA level change |
Protein level change |
Mutation effects |
Expt. name |
PubMed |
Mutation viewer |
| 1 |
Deletion |
- |
c.346_408del |
r.346_408del
|
p.Gly116_Ser136del |
Amino acid deletion |
Direct sequencing |
DiSanto JP et al., 1993
|
Click here |
| 2 |
Deletion |
- |
c.289_346del |
r.289_346del
|
p.Asp97ValfsX11 |
Frameshift |
Direct sequencing |
Pienaar S et al., 2003
|
Click here |
| 3 |
Substitution |
- |
c.-192A>C |
-
|
- |
Regulatory defects |
Direct sequencing |
Van Hoeyveld E et al., 2007
|
Click here |
| 4 |
Substitution |
g.103C>T |
c.31C>T |
-
|
p.Arg11X |
Nonsense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 5 |
Substitution |
g.103C>T |
c.31C>T |
-
|
p.Arg11X |
Nonsense defects |
Direct sequencing |
Blaeser F et al., 2005
|
Click here |
| 6 |
Substitution |
g.103C>T |
c.31C>T |
-
|
p.Arg11X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 7 |
Substitution |
g.103C>T |
c.31C>T |
-
|
p.Arg11X |
Nonsense defects |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 8 |
Substitution |
g.103C>T |
c.31C>T |
-
|
p.Arg11X |
Nonsense defects |
Direct sequencing, PCR based assay |
Yong PF et al., 2008
|
Click here |
| 9 |
Insertion |
g.136_137ins292 |
c.64_65ins292 |
r.64_65ins292
|
p.Met25PhefsX60 |
Frameshift |
Direct sequencing |
Apoil PA et al., 2007
|
Click here |
| 10 |
Substitution |
g.150T>G |
c.78T>G |
-
|
p.Tyr26X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 11 |
Deletion |
g.155delT |
c.83delT |
-
|
p.Thr29LeufsX8 |
Frameshift |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 12 |
Substitution |
g.179T>G |
c.107T>G |
-
|
p.Met36Arg |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 13 |
Substitution |
g.179T>G |
c.107T>G |
-
|
p.Met36Arg |
Missense defects |
Direct sequencing |
Korthauer U et al., 1993
|
Click here |
| 14 |
Substitution |
g.179T>G |
c.107T>G |
-
|
p.Met36Arg |
Missense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 15 |
Substitution |
g.184G>C |
c.112G>C |
-
|
p.Gly38Arg |
Missense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 16 |
Substitution |
g.184G>C |
c.112G>C |
-
|
p.Gly38Arg |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 17 |
Substitution |
g.188C>G |
c.116C>G |
-
|
p.Ser39X |
Nonsense defects |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 18 |
Substitution |
g.214A>T |
c.142A>T |
-
|
p.Arg48X |
Nonsense defects |
Direct sequencing |
Weller S et al., 2001
|
Click here |
| 19 |
Substitution |
g.226A>T |
c.154A>T |
-
|
p.Lys52X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 20 |
Substitution |
g.229G>A |
c.156+1G>A |
-
|
- |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 21 |
Substitution |
g.229G>T |
c.156+1G>T |
-
|
- |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 22 |
Substitution |
g.229G>T |
c.156+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Lin Q et al., 1996
|
Click here |
| 23 |
Substitution |
g.230T>C |
c.156+2T>C |
-
|
- |
Splice donor defects |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 24 |
Deletion |
g.2085_2093delAATAGATAG |
c.157-5_160delAATAGATAG |
-
|
- |
Amino acid deletion |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 25 |
Deletion |
g.2086_2093delATAGATAG |
c.157-4_160delATAGATAG |
-
|
- |
Amino acid deletion |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 26 |
Deletion |
g.2090_2093delATAG |
c.157_160delATAG |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 27 |
Deletion |
g.2090_2093delATAG |
c.157_160delATAG |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 28 |
Deletion |
g.2090_6217del |
c.157_288del |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 29 |
Deletion |
g.2090_2093delATAG |
c.157_160delATAG |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 30 |
Deletion |
g.2090_2093delATAG |
c.157_160delATAG |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing, PCR based assay |
Rangel-Santos A et al., 2009
|
Click here |
| 31 |
Deletion |
g.2090_2093delATAG |
c.157_160delATAG |
-
|
p.Ile53LysfsX13 |
Frameshift |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 32 |
Deletion |
g.2091_2094delTAGA |
c.158_161delTAGA |
-
|
p.Ile53fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 33 |
Substitution |
g.2099G>T |
c.166G>T |
-
|
p.Glu56X |
Nonsense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 34 |
Substitution |
g.2099G>T |
c.166G>T |
-
|
p.Glu56X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 35 |
Deletion |
g.2113_2129del |
c.180_196del |
-
|
p.Glu61fs |
Frameshift |
Direct sequencing |
Rezaei N et al., 2008
|
Click here |
| 36 |
Deletion |
g.2113_2129del17 |
c.180_196del17 |
-
|
p.Asp62Asnfs |
Frameshift |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 37 |
Duplications |
g.2122dupT |
c.189dupT |
-
|
p.Val64CysfsX21 |
Frameshift |
Direct sequencing |
Kraakman ME et al., 1995
|
Click here |
| 38 |
Duplications |
g.2136dupC |
c.203dupC |
-
|
p.Ile69AspfsX16 |
Frameshift |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 39 |
Substitution |
g.2141C>T |
c.208C>T |
-
|
p.Gln70X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 40 |
Deletion |
g.2141_2142delCA |
c.208_209delCA |
-
|
p.Gln70fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 41 |
Substitution |
g.2149C>A |
c.216C>A |
-
|
p.Cys72X |
Nonsense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 42 |
Substitution |
g.2149C>A |
c.216C>A |
-
|
p.Cys72X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 43 |
Substitution |
g.2159G>T |
c.226G>T |
-
|
p.Glu76X |
Nonsense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 44 |
Insertion |
g.2175_2176insT |
c.242_243insT |
-
|
p.Leu81fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 45 |
Deletion |
g.2204_2210delTTTGAAG |
c.271_277delTTTGAAG |
-
|
p.Phe91fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 46 |
Substitution |
g.2219A>T |
c.286A>T |
-
|
p.Lys96X |
Nonsense defects |
Direct sequencing |
Ma YC et al., 2005
|
Click here |
| 47 |
Substitution |
g.2221G>C |
c.288G>C |
-
|
p.Lys96Asn |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 48 |
Substitution |
g.2222G>A |
c.288+1G>A |
r.157_288del
|
p.Ile157_Gly288del |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 49 |
Substitution |
g.2223T>A |
c.288+2T>A |
r.157_288del
|
p.Ile157_Gly288del |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 50 |
Substitution |
g.2226G>A |
c.288+5G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Lin Q et al., 1996
|
Click here |
| 51 |
Substitution |
g.5340A>T |
c.347-915A>T |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 52 |
Substitution |
g.5340A>T |
c.347-915A>T |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Gilmour KC et al., 2003
|
Click here |
| 53 |
Deletion |
g.6197_6254del57 |
c.289_346del57 |
-
|
- |
Exon skipping |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 54 |
Deletion |
g.6203delA |
c.295delA |
-
|
p.Met99fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 55 |
Insertion |
g.6210_6211insA |
c.302_303insA |
-
|
p.Asn101fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 56 |
Substitution |
g.6230G>T |
c.322G>T |
-
|
p.Glu108X |
Nonsense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 57 |
Substitution |
g.6242G>T |
c.334G>T |
-
|
p.Glu112X |
Nonsense defects |
Dideoxy fingerprinting, PCR based assay |
Garcia-Perez MA et al., 2003
|
Click here |
| 58 |
Deletion |
g.6251_6254delAAAG |
c.343_346delAAAG |
-
|
p.Lys115fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 59 |
Deletion |
g.6253_6259delAGGTGAT |
c.345_351delAGGTGAT |
-
|
p.Lys115fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 60 |
Substitution |
g.6254G>C |
c.346G>C |
r.346g>c
|
p.Lys96AsnfsX12 |
Exon skipping, Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 61 |
Substitution |
g.6255G>T |
c.346+1G>T |
-
|
- |
Splice donor defects, Exon skipping |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 62 |
Substitution |
g.6255G>A |
c.346+1G>A |
r.289_346del
|
p.Gly116ValfsX12 |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 63 |
Deletion |
g.6255delG |
c.346+1delG |
r.289_346del
|
p.Gly116ValfsX12 |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 64 |
Substitution |
g.6255G>T |
c.346+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Gilmour KC et al., 2003
|
Click here |
| 65 |
Substitution |
g.6256T>C |
c.346+2T>C |
-
|
- |
Splice donor defects, Exon skipping |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 66 |
Substitution |
g.6256T>C |
c.346+2T>C |
r.289_346del
|
p.Gly116ValfsX12 |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 67 |
Substitution |
g.6259G>C |
c.346+5G>C |
r.289_346del
|
p.Gly116ValfsX12 |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 68 |
Substitution |
g.6259G>T |
c.346+5G>T |
r.289_346del
|
p.Gly116ValfsX12 |
Exon skipping |
SSCP |
Lopez-Granados E et al., 2003
|
Click here |
| 69 |
Substitution |
g.8179G>A |
c.347-1G>A |
r.347_409del
|
p.Gly116_Val137del |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 70 |
Substitution |
g.8179G>C |
c.347-1G>C |
r.347_409del
|
p.Gly116_Val137del |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 71 |
Substitution |
g.8179G>A |
c.347-1G>A |
-
|
- |
Splice acceptor defects |
Dideoxy fingerprinting, PCR based assay |
Garcia-Perez MA et al., 2003
|
Click here |
| 72 |
Deletion |
g.8180_10862del |
c.347_409del |
-
|
p.Gly116fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 73 |
Substitution |
g.8201C>A |
c.368C>A |
-
|
p.Ala123Glu |
Missense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 74 |
Substitution |
g.8201C>A |
c.368C>A |
r.368c>a
|
p.Ala123Glu |
Missense defects |
Direct sequencing |
DiSanto JP et al., 1993
|
Click here |
| 75 |
Deletion |
g.8202delG |
c.369delG |
-
|
p.Val126fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 76 |
Substitution |
g.8207A>G |
c.374A>G |
-
|
p.His125Arg |
Missense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 77 |
Substitution |
g.8210T>C |
c.377T>C |
-
|
p.Val126Ala |
Missense defects |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 78 |
Substitution |
g.8210T>A |
c.377T>A |
-
|
p.Val126Asp |
Missense defects |
Direct sequencing, PCR based assay |
Rangel-Santos A et al., 2009
|
Click here |
| 79 |
Substitution |
g.8210T>G |
c.377T>G |
-
|
p.Val126Gly |
Missense defects |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 80 |
Insertion |
g.8216insA |
c.383insA |
-
|
p.Ser128fs |
Frameshift |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 81 |
Substitution |
g.8217T>A |
c.384T>A |
-
|
p.Ser128Arg |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 82 |
Substitution |
g.8217T>A |
c.384T>A |
-
|
p.Ser128Arg |
Missense defects |
Direct sequencing |
Aruffo A et al., 1993
|
Click here |
| 83 |
Substitution |
g.8217T>A |
c.384T>A |
-
|
p.Ser128Arg |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 84 |
Insertion |
g.8217insG |
c.384insG |
-
|
p.Ser128fs |
Frameshift |
Direct sequencing |
Lin Q et al., 1996
|
Click here |
| 85 |
Substitution |
g.8219A>G |
c.386A>G |
-
|
p.Glu129Gly |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 86 |
Substitution |
g.8219A>G |
c.386A>G |
-
|
p.Glu129Gly |
Missense defects |
Direct sequencing |
Aruffo A et al., 1993
|
Click here |
| 87 |
Substitution |
g.8219A>G |
c.386A>G |
-
|
p.Glu129Gly |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 88 |
Deletion |
g.8242_8251delGTGTTACAGT |
c.409_418delGTGTTACAGT |
-
|
p.Val137fs |
Frameshift |
Direct sequencing |
Weller S et al., 2001
|
Click here |
| 89 |
Deletion |
g.8242_8251delGTGTTACAGT |
c.409_418delGTGTTACAGT |
r.409_418delguguuacagu
|
p.Val137fs |
Frameshift |
Direct sequencing |
DiSanto JP et al., 1993
|
Click here |
| 90 |
Substitution |
g.8243G>A |
c.409+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 91 |
Substitution |
g.8243G>C |
c.409+1G>C |
r.347_409del
|
p.Gly116_Val137del |
Exon skipping |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 92 |
Substitution |
g.8243G>C |
c.409+1G>C |
-
|
- |
Splice donor defects |
Direct sequencing |
Lin Q et al., 1996
|
Click here |
| 93 |
Substitution |
g.8243G>A |
c.409+1G>A |
-
|
- |
Splice donor defects |
Dideoxy fingerprinting |
Villa A et al., 1994
|
Click here |
| 94 |
Substitution |
g.8247G>C |
c.409+5G>C |
-
|
- |
- |
NA |
Tsai HY et al., 2012
|
Click here |
| 95 |
Deletion |
g.10862delG |
c.410-1delG |
-
|
- |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 96 |
Insertion |
g.10862_10863ins9 |
c.410-1_410ins9 |
-
|
- |
Splice donor defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 97 |
Insertion |
g.10862_10863ins12 |
c.410-1_410ins12 |
-
|
- |
Amino acid insertion |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 98 |
Substitution |
g.10862A>G |
c.410-1A>G |
-
|
- |
Splice acceptor defects |
Dideoxy fingerprinting |
Villa A et al., 1994
|
Click here |
| 99 |
Deletion-Insertion |
g.10862_10871delinsAA |
c.410-1_418delinsAA |
-
|
- |
Splice anomalies |
Dideoxy fingerprinting |
Villa A et al., 1994
|
Click here |
| 100 |
Deletion |
g.10864_10871delGTTACAGT |
c.411_418delGTTACAGT |
r.411_418delguuacagu
|
p.Leu138fs |
Frameshift |
Direct sequencing |
DiSanto JP et al., 1993
|
Click here |
| 101 |
Substitution |
g.10868C>T |
c.415C>T |
-
|
p.Gln139X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 102 |
Substitution |
g.10871T>C |
c.418T>C |
-
|
p.Trp140Arg |
Missense defects |
Direct sequencing |
Jo EK et al., 2002
|
Click here |
| 103 |
Substitution |
g.10871T>G |
c.418T>G |
-
|
p.Trp140Gly |
Missense defects |
Direct sequencing |
Korthauer U et al., 1993
|
Click here |
| 104 |
Substitution |
g.10871T>C |
c.418T>C |
-
|
p.Trp140Arg |
Missense defects |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 105 |
Substitution |
g.10871T>G |
c.418T>G |
-
|
p.Trp140Gly |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 106 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 107 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Saiki O et al., 1995
|
Click here |
| 108 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 109 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Korthauer U et al., 1993
|
Click here |
| 110 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 111 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing, SSCP |
Seyama K et al., 1996
|
Click here |
| 112 |
Substitution |
g.10872G>A |
c.419G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 113 |
Substitution |
g.10873G>T |
c.420G>T |
-
|
p.Trp140Cys |
Missense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 114 |
Substitution |
g.10873G>T |
c.420G>T |
-
|
p.Trp140Cys |
Missense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 115 |
Deletion |
g.10873_10880del8 |
c.420_427del8 |
-
|
p.Leu138fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 116 |
Substitution |
g.10873G>A |
c.420G>A |
-
|
p.Trp140X |
Nonsense defects |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 117 |
Substitution |
g.10873G>C |
c.420G>C |
-
|
p.Trp140Cys |
Missense defects |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 118 |
Substitution |
g.10873G>A |
c.420G>A |
-
|
p.Trp140X |
Nonsense defects |
NA |
Tsai HY et al., 2012
|
Click here |
| 119 |
Deletion |
g.10877_10882delGAAAAA |
c.424_429delGAAAAA |
-
|
p.Ala141fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 120 |
Deletion |
g.10883delG |
c.430delG |
-
|
p.Lys143fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 121 |
Substitution |
g.10884G>A |
c.431G>A |
-
|
p.Gly144Glu |
Missense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 122 |
Substitution |
g.10884G>A |
c.431G>A |
-
|
p.Gly144Glu |
Missense defects |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 123 |
Deletion |
g.10886_10888delTAC |
c.433_435delTAC |
-
|
p.Tyr145del |
Amino acid deletion |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 124 |
Substitution |
g.10888C>A |
c.435C>A |
-
|
p.Tyr145X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 125 |
Substitution |
g.10893C>A |
c.440C>A |
-
|
p.Thr147Asn |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 126 |
Substitution |
g.10893C>A |
c.440C>A |
-
|
p.Thr147Asn |
Missense defects |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 127 |
Substitution |
g.10894C>A |
c.441C>A |
-
|
p.Thr147Asn |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 128 |
Deletion-Insertion |
g.10897_10901delinsC |
c.444_448delinsC |
-
|
p.Met148fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 129 |
Deletion-Insertion |
g.10897_10901delinsC |
c.444_448delinsC |
-
|
p.Met148fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 130 |
Deletion |
g.10897delG |
c.444delG |
-
|
p.Met148fs |
Frameshift |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 131 |
Substitution |
g.10917T>C |
c.464T>C |
-
|
p.Leu155Pro |
Missense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 132 |
Substitution |
g.10917T>C |
c.464T>C |
-
|
p.Leu155Pro |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 133 |
Substitution |
g.10917T>C |
c.464T>C |
-
|
p.Leu155Pro |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 134 |
Substitution |
g.10917T>C |
c.464T>C |
-
|
p.Leu155Pro |
Missense defects |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 135 |
Substitution |
g.10917T>C |
c.464T>C |
-
|
p.Leu155Pro |
Missense defects |
Direct sequencing |
Allen RC et al., 1993
|
Click here |
| 136 |
Deletion |
g.10923delA |
c.470delA |
-
|
p.Asn157fs |
Frameshift |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 137 |
Substitution |
g.10935T>G |
c.482T>G |
-
|
p.Leu161Arg |
Missense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 138 |
Substitution |
g.10935T>C |
c.482T>C |
-
|
p.Leu161Pro |
Missense defects |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 139 |
Insertion |
g.10947_10948insAA |
c.494_495insAA |
-
|
p.Arg165LysfsX26 |
Frameshift |
Direct sequencing |
Cabral-Marques O et al., 2012
|
Click here |
| 140 |
Substitution |
g.10949C>T |
c.496C>T |
-
|
p.Gln166X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 141 |
Substitution |
g.10952G>T |
c.499G>T |
-
|
p.Gly167X |
Nonsense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 142 |
Substitution |
g.10952G>C |
c.499G>C |
-
|
p.Gly167Arg |
Missense defects |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 143 |
Substitution |
g.10958T>G |
c.505T>G |
-
|
p.Tyr169Asn |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 144 |
Substitution |
g.10958T>A |
c.505T>A |
-
|
p.Tyr169Asn |
Missense defects |
Direct sequencing |
Lin SC et al., 2005
|
Click here |
| 145 |
Substitution |
g.10958T>A |
c.505T>A |
-
|
p.Tyr169Asn |
Missense defects |
Direct sequencing, PCR based assay |
Lin SC et al., 2006
|
Click here |
| 146 |
Deletion |
g.10961_10969del |
c.508_516del |
-
|
p.Tyr170fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 147 |
Substitution |
g.10962A>G |
c.509A>G |
-
|
p.Tyr170Cys |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 148 |
Deletion |
g.10964_10966delATC |
c.511_513delATC |
-
|
p.Ile171del |
Amino acid deletion |
SSCP |
Andrews FJ et al., 1996
|
Click here |
| 149 |
Deletion |
g.10964_10966delATC |
c.511_513delATC |
-
|
p.Ile171fs |
Frameshift |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 150 |
Deletion |
g.10964_10965delAT |
c.511_512delAT |
-
|
p.Ile171fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 151 |
Substitution |
g.10973C>T |
c.520C>T |
-
|
p.Gln174X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 152 |
Substitution |
g.10974A>G |
c.521A>G |
-
|
p.Gln174Arg |
Missense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 153 |
Substitution |
g.10974A>G |
c.521A>G |
-
|
p.Gln174Arg |
Missense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 154 |
Substitution |
g.10974A>G |
c.521A>G |
-
|
p.Gln174Arg |
Missense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 155 |
Deletion |
g.10974_10975delAA |
c.521_522delAA |
-
|
p.Gln174fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 156 |
Substitution |
g.10974A>G |
c.521A>G |
-
|
p.Gln174Arg |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 157 |
Deletion |
g.10992delA |
c.539delA |
-
|
p.Asn180fs |
Frameshift |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 158 |
Substitution |
g.11004C>A |
c.551C>A |
-
|
p.Ser184X |
Nonsense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 159 |
Substitution |
g.11009C>T |
c.556C>T |
-
|
p.Gln186X |
Nonsense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 160 |
Substitution |
g.11009C>T |
c.556C>T |
-
|
p.Gln186X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 161 |
Duplications |
g.11026_11030dupCAGCC |
c.573_577dupCAGCC |
-
|
p.Leu193fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 162 |
Insertion |
g.11034_11035insCT |
c.581_582insCT |
-
|
p.Cys194fs |
Frameshift |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 163 |
Deletion |
g.11042_11048delTCCCCCG |
c.589_595delTCCCCCG |
-
|
p.Lys196fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 164 |
Substitution |
g.11051A>T |
c.598A>T |
-
|
p.Arg200X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 165 |
Substitution |
g.11051A>T |
c.598A>T |
-
|
p.Arg200X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 166 |
Substitution |
g.11061G>T |
c.608G>T |
-
|
p.Arg203Ile |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 167 |
Substitution |
g.11085C>A |
c.632C>A |
-
|
p.Thr211Asn |
Missense defects |
Direct sequencing |
Allen RC et al., 1993
|
Click here |
| 168 |
Deletion |
g.11089_11090delCA |
c.636_637delCA |
-
|
p.His212_Ser213del |
Amino acid deletion |
Direct sequencing |
Saiki O et al., 1995
|
Click here |
| 169 |
Deletion |
g.11089_11090delCA |
c.636_637delCA |
-
|
p.His212fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 170 |
Substitution |
g.11107C>A |
c.654C>A |
-
|
p.Cys218X |
Nonsense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 171 |
Substitution |
g.11107C>A |
c.654C>A |
-
|
p.Cys218X |
Nonsense defects |
Direct sequencing |
Prasad ML et al., 2005
|
Click here |
| 172 |
Substitution |
g.11107C>A |
c.654C>A |
-
|
p.Cys218X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 173 |
Substitution |
g.11107C>A |
c.654C>A |
-
|
p.Cys218X |
Nonsense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 174 |
Substitution |
g.11107C>A |
c.654C>A |
-
|
p.Cys218X |
Nonsense defects |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 175 |
Substitution |
g.11111C>T |
c.658C>T |
-
|
p.Gln220X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 176 |
Substitution |
g.11111C>T |
c.658C>T |
-
|
p.Gln220X |
Nonsense defects |
PCR based assay, Restriction enzyme analysis |
Jayoussi-Assalia R et al., 2000
|
Click here |
| 177 |
Substitution |
g.11114C>T |
c.661C>T |
-
|
p.Gln221X |
Nonsense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 178 |
Substitution |
g.11114C>T |
c.661C>T |
-
|
p.Gln221X |
Nonsense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 179 |
Substitution |
g.11114C>T |
c.661C>T |
-
|
p.Gln221X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 180 |
Substitution |
g.11119C>T |
c.666C>T |
-
|
p.Ser222Phe |
Missense defects |
SSCP |
Lopez-Granados E et al., 2003
|
Click here |
| 181 |
Deletion |
g.11132_11134delGGA |
c.679_681delGGA |
-
|
p.Gly227fs |
Frameshift |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 182 |
Substitution |
g.11132G>T |
c.679G>T |
-
|
p.Gly227X |
Nonsense defects |
Direct sequencing, PCR based assay |
Rangel-Santos A et al., 2009
|
Click here |
| 183 |
Substitution |
g.11133G>T |
c.680G>T |
-
|
p.Gly227Val |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 184 |
Substitution |
g.11133G>T |
c.680G>T |
-
|
p.Gly227Val |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 185 |
Substitution |
g.11133G>T |
c.680G>T |
-
|
p.Gly227Val |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 186 |
Substitution |
g.11133G>T |
c.680G>T |
-
|
p.Gly227Val |
Missense defects |
Direct sequencing |
Allen RC et al., 1993
|
Click here |
| 187 |
Insertion |
g.11140_11143insATTT |
c.687_690insATTT |
-
|
p.Glu230fs |
Frameshift |
Direct sequencing, PCR based assay |
Macchi P et al., 1995
|
Click here |
| 188 |
Substitution |
g.11140T>A |
c.687T>A |
-
|
p.Phe229Leu |
Missense defects |
Direct sequencing, PCR based assay |
Rangel-Santos A et al., 2009
|
Click here |
| 189 |
Substitution |
g.11145T>C |
c.692T>C |
-
|
p.Leu231Ser |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 190 |
Substitution |
g.11145T>C |
c.692T>C |
-
|
p.Leu231Ser |
Missense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 191 |
Substitution |
g.11146G>T |
c.693G>T |
-
|
p.Leu231Ser |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 192 |
Substitution |
g.11147C>T |
c.694C>T |
-
|
p.Gln232X |
Nonsense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 193 |
Substitution |
g.11147C>T |
c.694C>T |
-
|
p.Gln232X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Lin Q et al., 1996
|
Click here |
| 194 |
Substitution |
g.11147C>T |
c.694C>T |
-
|
p.Gln232X |
Nonsense defects |
Direct sequencing |
Erdos M et al., 2008
|
Click here |
| 195 |
Deletion |
g.11152_11154delAGG |
c.699_701delAGG |
-
|
p.Pro233fs |
Frameshift |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 196 |
Substitution |
g.11156G>C |
c.703G>C |
-
|
p.Ala235Pro |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 197 |
Substitution |
g.11156G>C |
c.703G>C |
-
|
p.Ala235Pro |
Missense defects |
Direct sequencing |
Aruffo A et al., 1993
|
Click here |
| 198 |
Substitution |
g.11156G>C |
c.703G>C |
-
|
p.Ala235Pro |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 199 |
Substitution |
g.11160C>A |
c.707C>A |
-
|
p.Ser236X |
Nonsense defects |
Direct sequencing |
Weller S et al., 2001
|
Click here |
| 200 |
Substitution |
g.11163T>A |
c.710T>A |
-
|
p.Val237Glu |
Missense defects |
Direct sequencing |
Saiki O et al., 1995
|
Click here |
| 201 |
Substitution |
g.11210T>A |
c.757T>A |
-
|
p.Phe253Ile |
Missense defects |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 202 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 203 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
| 204 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing |
Nonoyama S et al., 1997
|
Click here |
| 205 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 206 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 207 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Fluorescent sequencing |
de Vries E et al., 1999
|
Click here |
| 208 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Fluorescent sequencing |
Danielian S et al., 2007
|
Click here |
| 209 |
Substitution |
g.11214C>T |
c.761C>T |
-
|
p.Thr254Met |
Missense defects |
Direct sequencing |
Aghamohammadi A et al., 2009
|
Click here |
| 210 |
Substitution |
g.11222G>A |
c.769G>A |
-
|
p.Gly257Ser |
Missense defects |
Direct sequencing, SSCP |
Katz F et al., 1996
|
Click here |
| 211 |
Substitution |
g.11222G>A |
c.769G>A |
-
|
p.Gly257Ser |
Missense defects |
Direct sequencing, SSCP |
Gilmour KC et al., 2003
|
Click here |
| 212 |
Substitution |
g.11223G>T |
c.770G>T |
r.770g>u
|
p.Gly257Val |
Missense defects |
PCR based assay |
Heinold A et al., 2010
|
Click here |
| 213 |
Substitution |
g.11226T>C |
c.773T>C |
-
|
p.Leu258Ser |
Missense defects |
Direct sequencing |
Seyama K et al., 1998
|
Click here |
| 214 |
Substitution |
g.11226T>C |
c.773T>C |
-
|
p.Leu258Ser |
Missense defects |
Direct sequencing |
Lee WI et al., 2005
|
Click here |
|