| Sl.No |
Mutation type |
Genomic level change |
CDS level change |
RNA level change |
Protein level change |
Mutation effects |
Expt. name |
PubMed |
Mutation viewer |
| 1 |
Substitution |
g.366T>C |
c.20T>C |
-
|
p.Leu7Pro |
Missense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 2 |
Substitution |
g.377G>A |
c.30+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 3 |
Deletion |
g.12514_12515delGC |
c.46_47delGC |
-
|
p.Ala16X |
Nonsense defects |
Direct sequencing, PCR based assay |
Vaishnaw AK et al., 1999
|
Click here |
| 4 |
Deletion |
g.12514_12515delGC |
c.46_47delGC |
-
|
p.Ala16X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 5 |
Substitution |
g.12521T>G |
c.53T>G |
-
|
p.Leu18X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 6 |
Substitution |
g.12568G>T |
c.100G>T |
-
|
p.Gly34X |
Nonsense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 7 |
Insertion |
g.12592insA |
c.124insA |
-
|
p.Thr42AsnfsX4 |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 8 |
Substitution |
g.12601G>T |
c.133G>T |
-
|
p.Glu45X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 9 |
Substitution |
g.12607C>T |
c.139C>T |
-
|
p.Gln47X |
Nonsense defects |
Direct sequencing |
Cerutti E et al., 2007
|
Click here |
| 10 |
Substitution |
g.12607C>T |
c.139C>T |
-
|
p.Gln47X |
Nonsense defects |
NA |
Campagnoli MF et al., 2006
|
Click here |
| 11 |
Duplications |
g.12634_12640dupGGCCAAT |
c.166_172dupGGCCAAT |
-
|
p.Phe58fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 12 |
Substitution |
g.12657T>A |
c.189T>A |
-
|
p.Cys63X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 13 |
Substitution |
g.17169G>A |
c.197-1G>A |
-
|
p.Pro65_Gly110del |
Splice acceptor defects, Amino acid deletion |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 14 |
Substitution |
g.17192C>A |
c.219C>A |
-
|
p.Cys73X |
Nonsense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 15 |
Substitution |
g.17192C>A |
c.219C>A |
-
|
p.Cys73X |
Nonsense defects |
Direct sequencing |
Sneller MC et al., 1997
|
Click here |
| 16 |
Deletion |
g.17208delG |
c.235delG |
-
|
p.Glu79AsnfsX35 |
Frameshift |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 17 |
Deletion |
g.17208delG |
c.235delG |
-
|
p.Glu79AsnfsX35 |
Frameshift |
Direct sequencing |
Fisher GH et al., 1995
|
Click here |
| 18 |
Substitution |
g.17208G>T |
c.235G>T |
r.235g>u
|
p.Glu79X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 19 |
Substitution |
g.17217T>C |
c.244T>C |
-
|
p.Cys82Arg |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 20 |
Deletion |
g.17225_17229delCTGCC |
c.252_256delCTGCC |
-
|
p.Cys85ArgfsX19 |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 21 |
Substitution |
g.17246C>A |
c.273C>A |
-
|
p.Tyr91X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 22 |
Substitution |
g.17283T>G |
c.310T>G |
-
|
p.Cys104Gly |
Missense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 23 |
Substitution |
g.17293G>A |
c.320G>A |
-
|
p.Cys107Tyr |
Missense defects |
Direct sequencing |
Simesen de Bielke MG et al., 2012
|
Click here |
| 24 |
Substitution |
g.17293G>A |
c.320G>A |
-
|
p.Cys107Tyr |
Missense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 25 |
Substitution |
g.17296A>G |
c.323A>G |
-
|
p.Asp108Gly |
Missense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 26 |
Deletion |
g.17297_17299delTGA |
c.324_326delTGA |
-
|
p.Asp108del |
Amino acid deletion |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 27 |
Substitution |
g.17305A>C |
c.332A>C |
-
|
p.His111Pro |
Missense defects |
NA |
Campagnoli MF et al., 2006
|
Click here |
| 28 |
Substitution |
g.17305A>G |
c.332A>G |
-
|
p.His111Arg |
Missense defects |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 29 |
Substitution |
g.17305A>G |
c.332A>G |
-
|
p.His111Arg |
Missense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 30 |
Duplications |
g.17309dupT |
c.334+2dupT |
r.[197_334del,197_443del; 334+2dupu]
|
p.[Glu67_Gly112del, Gly66AspfsX39] |
Splice donor defects, Amino acid deletion, Exon skipping, Frameshift |
Direct sequencing |
Fisher GH et al., 1995
|
Click here |
| 31 |
Substitution |
g.18357A>G |
c.335-2A>G |
-
|
p.Gly112AspfsX39 |
Splice acceptor defects, Exon skipping, Frameshift |
Direct sequencing |
Cerutti E et al., 2007
|
Click here |
| 32 |
Substitution |
g.18371A>G |
c.347A>G |
-
|
p.Glu116Gly |
Missense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 33 |
Substitution |
g.18377A>G |
c.353A>G |
-
|
p.Asn118Ser |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Lee SH et al., 2000
|
Click here |
| 34 |
Substitution |
g.18385C>T |
c.361C>T |
-
|
p.Arg121Trp |
Missense defects |
Direct sequencing |
Bettinardi A et al., 1997
|
Click here |
| 35 |
Deletion-Insertion |
g.18421_18422delTTinsA |
c.397_398delTTinsA |
-
|
p.Phe133Ilefs |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 36 |
Substitution |
g.18428G>A |
c.404G>A |
-
|
p.Cys135Tyr |
Missense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 37 |
Substitution |
g.18472G>A |
c.443+5G>A |
-
|
p.Gly66Aspfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 38 |
Substitution |
g.20008G>C |
c.444-1G>C |
-
|
p.Cys149AsnfsX31 |
Frameshift |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 39 |
Substitution |
g.20036C>A |
c.471C>A |
-
|
p.Cys157X |
Nonsense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 40 |
Deletion-Insertion |
g.20040_20054delinsA |
c.475_489delinsA |
-
|
p.Leu159LysfsX10 |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 41 |
Substitution |
g.20207A>G |
c.506-16A>G |
-
|
p.Gly169_Trp189del |
Amino acid deletion, Splice acceptor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 42 |
Substitution |
g.20217C>G |
c.506-6C>G |
-
|
p.Gly169_Trp189del |
Amino acid deletion |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 43 |
Substitution |
g.20220C>G |
c.506-3C>G |
-
|
- |
Exon skipping |
Direct sequencing |
Roesler J et al., 2005
|
Click here |
| 44 |
Deletion |
g.20223-?_20285+?del |
c.506-?_568+?del |
-
|
- |
Exon skipping |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 45 |
Deletion |
g.20239delGGGG |
c.522delGGGG |
-
|
p.Leu174PhefsX12 |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 46 |
Substitution |
g.20245G>A |
c.528G>A |
-
|
p.Trp176X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 47 |
Substitution |
g.20249T>C |
c.532T>C |
-
|
p.Cys178Arg |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Lee SH et al., 2000
|
Click here |
| 48 |
Substitution |
g.21464T>G |
c.569-5T>G |
-
|
p.Val190GlyfsX7 |
Frameshift, Splice acceptor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 49 |
Substitution |
g.21467A>C |
c.569-2A>C |
-
|
p.Lys191X |
Splice acceptor defects, Nonsense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 50 |
Substitution |
g.21467A>C |
c.569-2A>C |
r.568_569ins569-72_569-1
|
p.Lys191X |
Splice acceptor defects, Nonsense defects |
Direct sequencing |
Fisher GH et al., 1995
|
Click here |
| 51 |
Substitution |
g.21480G>A |
c.580G>A |
-
|
p.Glu194Lys |
Missense defects |
NA |
Campagnoli MF et al., 2006
|
Click here |
| 52 |
Deletion |
g.21485_21495del11 |
c.585_595del11 |
-
|
p.Thr198AlafsX10 |
Frameshift |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 53 |
Insertion |
g.21485insA |
c.585insA |
-
|
p.Gln196ThrfsX16 |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 54 |
Substitution |
g.21507A>T |
c.607A>T |
-
|
p.Arg203X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 55 |
Substitution |
g.21531G>T |
c.631G>T |
-
|
p.Glu211X |
Nonsense defects |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 56 |
Substitution |
g.21552G>A |
c.651+1G>A |
-
|
p.Val190Glyfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 57 |
Substitution |
g.21553T>A |
c.651+2T>A |
-
|
p.Pro217fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 58 |
Substitution |
g.21553T>A |
c.651+2T>A |
-
|
p.Val190Glyfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 59 |
Substitution |
g.21556G>T |
c.651+5G>T |
-
|
p.Val190Glyfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 60 |
Deletion |
g.22804_22814del11 |
c.652-9_653del11 |
-
|
p.Glu218MetfsX4 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 61 |
Substitution |
g.22812G>T |
c.652-1G>T |
-
|
p.Glu218MetfsX4 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 62 |
Substitution |
g.22812G>A |
c.652-1G>A |
-
|
p.Glu218MetfsX4 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 63 |
Substitution |
g.22813G>A |
c.652G>A |
-
|
p.Pro217fs |
Exon skipping, Frameshift |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 64 |
Substitution |
g.22813G>T |
c.652G>T |
r.652g>u
|
p.Glu218X |
Nonsense defects |
Allele-specific oligonucleotide hybridization analysis, Direct sequencing, PCR based assay |
Holzelova E et al., 2004
|
Click here |
| 65 |
Deletion |
g.22818_22819delAG |
c.657_658delAG |
-
|
p.Val220GlyfsX6 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 66 |
Deletion |
g.22829_22836del8 |
c.668_675del8 |
-
|
p.Asn223ArgfsX3 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 67 |
Substitution |
g.22832T>G |
c.671T>G |
-
|
p.Leu224X |
Nonsense defects |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 68 |
Substitution |
g.22837G>T |
c.676G>T |
-
|
p.Glu218MetfsX4 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 69 |
Substitution |
g.22838G>A |
c.676+1G>A |
r.[=,652_676del; 676+1g>a]
|
p.Glu218MetfsX4 |
Frameshift, Exon skipping |
Allele-specific oligonucleotide hybridization analysis, Direct sequencing, PCR based assay |
Holzelova E et al., 2004
|
Click here |
| 70 |
Substitution |
g.22838G>A |
c.676+1G>A |
-
|
p.Glu218MetfsX4 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 71 |
Substitution |
g.22838G>A |
c.676+1G>A |
-
|
p.Glu218Metfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 72 |
Substitution |
g.22838G>T |
c.676+1G>T |
-
|
p.Glu218Metfs |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 73 |
Substitution |
g.22839T>C |
c.676+2T>C |
r.[=,652_676del; 676+2u>c]
|
p.Glu218Metfs |
Frameshift, Splice donor defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 74 |
Substitution |
g.22839T>C |
c.676+2T>C |
-
|
p.Glu218Metfs |
Frameshift, Splice donor defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 75 |
Substitution |
g.23581T>G |
c.677-8T>G |
-
|
p.Asp226fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 76 |
Substitution |
g.23589A>G |
c.677A>G |
-
|
p.Asp226Gly |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 77 |
Deletion |
g.23594_23598del5 |
c.682_686del5 |
-
|
p.Asp228GlufsX2 |
Frameshift |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 78 |
Deletion-Insertion |
g.23598_23606delTGAGTAAATinsGAG |
c.686_694delTGAGTAAATinsGAG |
-
|
p.Leu229X |
Nonsense defects |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
| 79 |
Insertion |
g.23604_23605insT |
c.692_693insT |
r.692_693insu
|
p.Lys231fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Drappa J et al., 1996
|
Click here |
| 80 |
Substitution |
g.23607A>G |
c.695A>G |
-
|
p.Tyr232Cys |
Missense defects |
Direct sequencing |
Bettinardi A et al., 1997
|
Click here |
| 81 |
Deletion |
g.23620_23623delTGCT |
c.708_711delTGCT |
-
|
p.Ile236MetfsX4 |
Frameshift |
Denaturing gradient gel electrophoresis, Direct sequencing |
Gualco G et al., 2008
|
Click here |
| 82 |
Substitution |
g.23621G>C |
c.709G>C |
-
|
p.Ala237Pro |
Missense defects |
Direct sequencing |
Magerus-Chatinet A et al., 2011
|
Click here |
| 83 |
Substitution |
g.23633A>C |
c.721A>C |
-
|
p.Thr241Pro |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 84 |
Substitution |
g.23633A>C |
c.721A>C |
-
|
p.Thr241Pro |
Missense defects |
Direct sequencing |
Fisher GH et al., 1995
|
Click here |
| 85 |
Substitution |
g.23634C>A |
c.722C>A |
-
|
p.Thr241Lys |
Missense defects |
Direct sequencing |
Aspinall AI et al., 1999
|
Click here |
| 86 |
Substitution |
g.23634C>A |
c.722C>A |
-
|
p.Thr241Lys |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 87 |
Duplications |
g.23639_23642dupAGTC |
c.727_730dupAGTC |
r.727_730dupaguc
|
p.Ser243fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 88 |
Substitution |
g.23657G>C |
c.745G>C |
r.745g>c
|
p.Val249Leu |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 89 |
Substitution |
g.23660C>T |
c.748C>T |
r.748c>u
|
p.Arg250X |
Nonsense defects |
Direct sequencing, PCR based assay, SSCP |
Drappa J et al., 1996
|
Click here |
| 90 |
Substitution |
g.23661G>A |
c.749G>A |
-
|
p.Arg250Gln |
Missense defects |
Direct sequencing |
van den Berg A et al., 2002
|
Click here |
| 91 |
Substitution |
g.23661G>A |
c.749G>A |
-
|
p.Arg250Gln |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 92 |
Substitution |
g.23661G>C |
c.749G>C |
-
|
p.Arg250Pro |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 93 |
Substitution |
g.23661G>C |
c.749G>C |
-
|
p.Arg250Pro |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 94 |
Substitution |
g.23661G>C |
c.749G>C |
r.749g>c
|
p.Arg250Pro |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 95 |
Substitution |
g.23661G>C |
c.749G>C |
-
|
p.Arg250Pro |
Missense defects |
Direct sequencing |
Kuijpers TW et al., 2011
|
Click here |
| 96 |
Substitution |
g.23669G>A |
c.757G>A |
r.757g>a
|
p.Gly253Ser |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 97 |
Substitution |
g.23670G>A |
c.758G>A |
r.758g>a
|
p.Gly253Asp |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 98 |
Substitution |
g.23673T>G |
c.761T>G |
-
|
p.Val254Gly |
Missense defects |
Sanger Sequencing |
Hansford JR et al., 2012
|
Click here |
| 99 |
Substitution |
g.23675A>G |
c.763A>G |
-
|
p.Asn255Asp |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Lee SH et al., 2000
|
Click here |
| 100 |
Substitution |
g.23682C>A |
c.770C>A |
-
|
p.Ala257Asp |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 101 |
Substitution |
g.23688T>G |
c.776T>G |
r.776u>g
|
p.Ile259Arg |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 102 |
Substitution |
g.23690G>A |
c.778G>A |
-
|
p.Asp260Asn |
Missense defects |
Direct sequencing, SSCP |
Mullauer L et al., 2008
|
Click here |
| 103 |
Substitution |
g.23690G>T |
c.778G>T |
r.778g>u
|
p.Asp260Tyr |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Drappa J et al., 1996
|
Click here |
| 104 |
Substitution |
g.23690G>A |
c.778G>A |
-
|
p.Asp260Asn |
Missense defects |
Direct sequencing |
Dowdell KC et al., 2010
|
Click here |
| 105 |
Substitution |
g.23691A>T |
c.779A>T |
-
|
p.Asp260Val |
Missense defects |
Direct sequencing |
Infante AJ et al., 1998
|
Click here |
| 106 |
Substitution |
g.23691A>T |
c.779A>T |
r.779a>u
|
p.Asp260Val |
Missense defects |
Direct sequencing, PCR based assay |
Holzelova E et al., 2004
|
Click here |
| 107 |
Deletion |
g.23721_23722delCA |
c.809_810delCA |
-
|
p.Thr270SerfsX10 |
Frameshift |
Direct sequencing |
Rieux-Laucat F et al., 1995
|
Click here |
| 108 |
Substitution |
g.23721C>T |
c.809C>T |
-
|
p.Thr270Ile |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Vaishnaw AK et al., 1999
|
Click here |
| 109 |
Substitution |
g.23721C>A |
c.809C>A |
r.809c>a
|
p.Thr270Lys |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 110 |
Substitution |
g.23726G>A |
c.814G>A |
r.814g>a
|
p.Glu272Lys |
Missense defects |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 111 |
Substitution |
g.23729C>T |
c.817C>T |
-
|
p.Gln273X |
Nonsense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 112 |
Substitution |
g.23729C>T |
c.817C>T |
-
|
p.Gln273X |
Nonsense defects |
Direct sequencing |
Fisher GH et al., 1995
|
Click here |
| 113 |
Substitution |
g.23731G>C |
c.819G>C |
-
|
p.Gln273His |
Missense defects |
NA |
Campagnoli MF et al., 2006
|
Click here |
| 114 |
Substitution |
g.23738C>T |
c.826C>T |
-
|
p.Gln276X |
Nonsense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 115 |
Deletion |
g.23792delT |
c.880delT |
-
|
p.Leu294X |
Nonsense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 116 |
Deletion |
g.23800delA |
c.888delA |
r.888dela
|
p.Asp297fs |
Frameshift |
Direct sequencing, PCR based assay, SSCP |
Rieux-Laucat F et al., 1999
|
Click here |
| 117 |
Substitution |
g.23841T>G |
c.929T>G |
-
|
p.Ile310Ser |
Missense defects |
Direct sequencing |
Jackson CE et al., 1999
|
Click here |
| 118 |
Substitution |
g.23841T>G |
c.929T>G |
-
|
p.Ile310Ser |
Missense defects |
Direct sequencing |
Sneller MC et al., 1997
|
Click here |
| 119 |
Duplications |
g.23880_23899dup20bp |
c.968_987dup20bp |
r.968_987dup20bp
|
p.Glu330fsLys |
Frameshift |
Direct sequencing, Heteroduplex analysis, PCR based assay, Southern blotting |
van der Burg M et al., 2000
|
Click here |
| 120 |
Deletion |
g.23897_23925del28 |
c.985_1008*4del28 |
-
|
p.Asn329Lysfs |
Frameshift |
Direct sequencing |
Hsu AP et al., 2012
|
Click here |
|