| 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.400-?_1260+?del |
-
|
- |
Amino acid deletion |
PCR based assay |
Zou CC et al., 2007
|
Click here |
| 2 |
Substitution |
g.5504G>T |
c.-4257G>T |
r.[=,(-4259-?)_(?+1)ins343, (-4259-?)_(?+1)del122]
|
- |
Regulatory defects |
Direct sequencing |
Mooster JL et al., 2010
|
Click here |
| 3 |
Insertion |
g.9869_9870insC |
c.110_111insC |
-
|
p.Ala37fs |
Frameshift |
Direct sequencing |
Niehues T et al., 2004
Puel A et al., 2006
Audry M et al., 2011
|
Click here |
| 4 |
Substitution |
g.9928G>A |
c.169G>A |
-
|
p.Glu57Lys |
Missense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 5 |
Substitution |
g.9943C>T |
c.184C>T |
-
|
p.Arg62X |
Nonsense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 6 |
Substitution |
g.13973T>C |
c.239T>C |
-
|
p.Leu80Pro |
Missense defects |
Direct sequencing |
Ku CL et al., 2005
|
Click here |
| 7 |
Deletion |
g.14000_14002delAGA |
c.266_268delAGA |
-
|
p.Lys90del |
Amino acid deletion |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 8 |
Substitution |
g.14071G>A |
c.337G>A |
-
|
p.Asp113Asn |
Missense defects |
Dideoxy fingerprinting, PCR based assay |
Salt BH et al., 2008
|
Click here |
| 9 |
Substitution |
g.14071G>A |
c.337G>A |
-
|
p.Asp113Asn |
Missense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 10 |
Substitution |
g.14101C>T |
c.367C>T |
-
|
p.Arg123Trp |
Missense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 11 |
Duplications |
g.16289-?_19541dup |
c.400-?_768dup |
-
|
p.Lys224fsX9 |
Frameshift |
Direct sequencing, Southern blotting |
Nishikomori R et al., 2004
|
Click here |
| 12 |
Substitution |
g.16326T>G |
c.437T>G |
-
|
p.Val146Gly |
Missense defects |
Direct sequencing |
Devora GA et al., 2010
|
Click here |
| 13 |
Substitution |
g.16347T>G |
c.458T>G |
-
|
p.Leu153Arg |
Missense defects |
Direct sequencing, PCR based assay |
Orange JS et al., 2002
|
Click here |
| 14 |
Substitution |
g.16347T>G |
c.458T>G |
-
|
p.Leu153Arg |
Missense defects |
Direct sequencing |
Orange JS et al., 2004
|
Click here |
| 15 |
Substitution |
g.16406C>G |
c.517C>G |
-
|
p.Arg173Gly |
Missense defects |
Direct sequencing |
Ku CL et al., 2007
|
Click here |
| 16 |
Substitution |
g.18169G>C |
c.524G>C |
-
|
p.Arg175Pro |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 17 |
Substitution |
g.19453T>C |
c.680T>C |
-
|
p.Leu227Pro |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 18 |
Substitution |
g.19488C>T |
c.715C>T |
-
|
p.Gln239X |
Nonsense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 19 |
Substitution |
g.19491G>T |
c.718G>T |
-
|
p.Glu240X |
Nonsense defects |
Direct sequencing |
Has C et al., 2007
|
Click here |
| 20 |
Substitution |
g.19546G>A |
c.768+5G>A |
r.400_768del
|
- |
Exon skipping, Splice donor defects |
Direct sequencing |
Orstavik KH et al., 2006
|
Click here |
| 21 |
Substitution |
g.20566G>C |
c.769-1G>C |
r.[768_769ins171, 768_769ins213, 768_769ins64, 768_769del51; 769-1g>c]
|
- |
Splice acceptor defects |
Direct sequencing, PCR based assay |
Karakawa S et al., 2011
|
Click here |
| 22 |
Duplications |
g.20590dupA |
c.792dupA |
-
|
p.Lys264fs |
Frameshift |
Direct sequencing |
Martinez-Pomar N et al., 2005
|
Click here |
| 23 |
Deletion |
g.20609_20626del |
c.811_828del |
-
|
p.Glu271fs |
Frameshift |
Direct sequencing |
Ku CL et al., 2005
|
Click here |
| 24 |
Substitution |
g.20661C>G |
c.863C>G |
-
|
p.Ala288Gly |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 25 |
Substitution |
g.21334G>A |
c.931G>A |
-
|
p.Asp311Asn |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
Hubeau M et al., 2011
|
Click here |
| 26 |
Substitution |
g.21335A>G |
c.932A>G |
-
|
p.Asp311Gly |
Missense defects |
Direct sequencing |
Hubeau M et al., 2011
|
Click here |
| 27 |
Substitution |
g.21336C>G |
c.933C>G |
r.933c>g
|
p.Asp311Glu |
Missense defects |
Direct sequencing |
Imamura M et al., 2011
|
Click here |
| 28 |
Insertion |
g.21346_21347insG |
c.943_944insG |
-
|
p.Glu315GlyfsX79 |
Frameshift |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 29 |
Substitution |
g.21346G>C |
c.943G>C |
-
|
p.Glu315Gln |
Missense defects |
Direct sequencing |
Hoshina T et al., 2011
|
Click here |
| 30 |
Substitution |
g.21347A>C |
c.944A>C |
-
|
p.Glu315Ala |
Missense defects |
Direct sequencing |
Filipe-Santos O et al., 2006
|
Click here |
| 31 |
Substitution |
g.21359G>A |
c.956G>A |
-
|
p.Arg319Gln |
Missense defects |
Direct sequencing |
Filipe-Santos O et al., 2006
|
Click here |
| 32 |
Substitution |
g.21370G>C |
c.967G>C |
-
|
p.Ala323Pro |
Missense defects |
Direct sequencing |
Sebban-Benin H et al., 2007
|
Click here |
| 33 |
Substitution |
g.21715G>A |
c.1056-1G>A |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Orange JS et al., 2004
|
Click here |
| 34 |
Substitution |
g.21715G>A |
c.1056-1G>A |
r.1056_1117del
|
- |
Exon skipping |
Direct sequencing, PCR based assay |
Orange JS et al., 2004
Puel A et al., 2006
|
Click here |
| 35 |
Substitution |
g.22108C>T |
c.1150C>T |
-
|
p.Gln384X |
Nonsense defects |
Denaturing HPLC, Direct sequencing |
Fusco F et al., 2004
|
Click here |
| 36 |
Duplications |
g.22119dupC |
c.1161dupC |
-
|
p.Glu390ArgfsX4 |
Frameshift |
Direct sequencing |
Kosaki K et al., 2001
|
Click here |
| 37 |
Deletion |
g.22119delC |
c.1161delC |
-
|
p.Glu390fs |
Frameshift |
CSGE, Direct sequencing |
Aradhya S et al., 2001
|
Click here |
| 38 |
Duplications |
g.22119dupC |
c.1161dupC |
-
|
p.Glu390ArgfsX5 |
Frameshift |
CSGE, Direct sequencing |
Aradhya S et al., 2001
|
Click here |
| 39 |
Deletion |
g.22121_22133del13 |
c.1163_1175del13 |
-
|
p.Pro388fs |
Frameshift |
CSGE, Direct sequencing |
Aradhya S et al., 2001
|
Click here |
| 40 |
Duplications |
g.22124_22136dup13 |
c.1166_1178dup13 |
-
|
p.Asp394ArgfsX5 |
Frameshift |
CSGE, Direct sequencing |
Aradhya S et al., 2001
|
Click here |
| 41 |
Duplications |
g.22125dupC |
c.1167dupC |
-
|
p.Glu390fs |
Frameshift |
Fluorescent sequencing |
Lee WI et al., 2005
|
Click here |
| 42 |
Insertion |
g.22125_22126insC |
c.1167_1168insC |
-
|
p.Glu390fs |
Frameshift |
Direct sequencing, PCR based assay |
Zonana J et al., 2000
|
Click here |
| 43 |
Insertion |
g.22125_22126insC |
c.1167_1168insC |
-
|
p.Glu390fs |
Frameshift |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 44 |
Duplications |
g.22125dupC |
c.1167dupC |
-
|
p.Glu390ArgfsX5 |
Frameshift |
Direct sequencing |
Schmid JM et al., 2006
|
Click here |
| 45 |
Duplications |
g.22125dupC |
c.1167dupC |
-
|
p.Glu390ArgfsX5 |
Frameshift |
Direct sequencing |
Mancini AJ et al., 2008
|
Click here |
| 46 |
Insertion |
g.22125_22126insC |
c.1167_1168insC |
-
|
p.Glu390ArgfsX5 |
Frameshift |
NA |
Tono C et al., 2007
|
Click here |
| 47 |
Duplications |
g.22125dupC |
c.1167dupC |
-
|
p.Glu390ArgfsX5 |
Frameshift |
NA |
Chang TT et al., 2008
|
Click here |
| 48 |
Substitution |
g.22129G>T |
c.1171G>T |
-
|
p.Glu391X |
Nonsense defects |
Direct sequencing, PCR based assay |
Zonana J et al., 2000
|
Click here |
| 49 |
Deletion |
g.22141_22142delTT |
c.1183_1184delTT |
-
|
p.Phe395LeufsX11 |
Frameshift |
Direct sequencing |
Roberts CM et al., 2010
|
Click here |
| 50 |
Substitution |
g.22165C>T |
c.1207C>T |
-
|
p.Gln403X |
Nonsense defects |
Direct sequencing, PCR based assay |
Orange JS et al., 2002
|
Click here |
| 51 |
Substitution |
g.22165C>T |
c.1207C>T |
-
|
p.Gln403X |
Nonsense defects |
Direct sequencing |
Orange JS et al., 2004
|
Click here |
| 52 |
Substitution |
g.22175A>T |
c.1217A>T |
-
|
p.Asp406Val |
Missense defects |
Direct sequencing |
Jain A et al., 2001
|
Click here |
| 53 |
Insertion |
g.22176_22177insA |
c.1218_1219insA |
-
|
p.Met407fs |
Frameshift |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 54 |
Substitution |
g.22207T>C |
c.1249T>C |
-
|
p.Cys417Arg |
Missense defects |
Direct sequencing, PCR based assay |
Zonana J et al., 2000
|
Click here |
| 55 |
Substitution |
g.22207T>C |
c.1249T>C |
-
|
p.Cys417Arg |
Missense defects |
Direct sequencing |
Jain A et al., 2001
|
Click here |
| 56 |
Substitution |
g.22207T>C |
c.1249T>C |
-
|
p.Cys417Arg |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 57 |
Substitution |
g.22207T>C |
c.1249T>C |
-
|
p.Cys417Arg |
Missense defects |
Direct sequencing, PCR based assay |
Orange JS et al., 2002
|
Click here |
| 58 |
Substitution |
g.22207T>C |
c.1249T>C |
-
|
p.Cys417Arg |
Missense defects |
Direct sequencing |
Orange JS et al., 2004
|
Click here |
| 59 |
Substitution |
g.22208G>T |
c.1250G>T |
-
|
p.Cys417Phe |
Missense defects |
Direct sequencing, PCR based assay |
Zonana J et al., 2000
|
Click here |
| 60 |
Substitution |
g.22208G>A |
c.1250G>A |
-
|
p.Cys417Tyr |
Missense defects |
Direct sequencing |
Orange JS et al., 2004
|
Click here |
| 61 |
Substitution |
g.22208G>T |
c.1250G>T |
-
|
p.Cys417Phe |
Missense defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 62 |
Substitution |
g.22217A>G |
c.1259A>G |
-
|
p.X420Trp |
Stop codon defects |
Direct sequencing, PCR based assay |
Doffinger R et al., 2001
|
Click here |
| 63 |
Substitution |
g.22217A>G |
c.1259A>G |
-
|
p.X420Trp |
Stop codon defects |
Direct sequencing, PCR based assay |
Mansour S et al., 2001
|
Click here |
|