| 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 |
- |
c.*876A>G |
-
|
- |
NA |
Fluorescent sequencing, PCR based assay |
Bennett CL et al., 2001
|
Click here |
| 2 |
Deletion |
g.80_1468del1388 |
- |
-
|
- |
Splice anomalies |
Fluorescent sequencing |
Torgerson TR et al., 2007
|
Click here |
| 3 |
Substitution |
g.6320G>T |
c.1-7G>T |
-
|
- |
Start codon defects |
Direct sequencing |
Myers AK et al., 2006
|
Click here |
| 4 |
Substitution |
g.6328T>C |
c.2T>C |
-
|
p.Met1Thr |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 5 |
Substitution |
g.6329G>A |
c.3G>A |
-
|
p.Met1Ile |
Missense defects |
Direct sequencing |
Bacchetta R et al., 2006
|
Click here |
| 6 |
Substitution |
g.6329G>A |
c.3G>A |
-
|
p.Met1Ile |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 7 |
Deletion-Insertion |
g.6536_6537delGGinsAC |
c.210_210+1delGGinsAC |
-
|
p.0 |
Splice anomalies |
Direct sequencing |
Gavin MA et al., 2006
|
Click here |
| 8 |
Substitution |
g.6538T>G |
c.210+2T>G |
-
|
- |
Splice donor defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 9 |
Deletion |
g.7080delT |
c.227delT |
-
|
p.Leu76GlnfsX53 |
Frameshift |
Direct sequencing |
Kobayashi I et al., 2001
|
Click here |
| 10 |
Deletion |
g.7080delT |
c.227delT |
-
|
p.Leu76GlnfsX53 |
Frameshift |
Direct sequencing, Restriction enzyme analysis |
Owen CJ et al., 2003
|
Click here |
| 11 |
Deletion |
g.7156_7157delTT |
c.303_304delTT |
-
|
p.Phe102fs |
Frameshift |
Direct sequencing |
Moudgil A et al., 2007
|
Click here |
| 12 |
Substitution |
g.7274C>T |
c.323C>T |
-
|
p.Thr108Met |
Missense defects |
Direct sequencing |
De Benedetti F et al., 2006
|
Click here |
| 13 |
Substitution |
g.7387C>T |
c.436C>T |
-
|
p.Arg146Trp |
Missense defects |
Direct sequencing |
Lee SM et al., 2009
|
Click here |
| 14 |
Substitution |
g.7409A>G |
c.454+4A>G |
r.[=,211_315del, 211_454del]
|
- |
Exon skipping |
Direct sequencing |
De Benedetti F et al., 2006
|
Click here |
| 15 |
Substitution |
g.7994C>T |
c.560C>T |
-
|
p.Pro187Leu |
Missense defects |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 16 |
Substitution |
g.9103T>C |
c.725T>C |
-
|
p.Leu242Pro |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 17 |
Substitution |
g.9318G>A |
c.736-1G>A |
-
|
p.Leu246_Val272del |
Splice acceptor defects, Amino acid deletion, Exon skipping |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 18 |
Deletion |
g.9331_9333delAAG |
c.748_750delAAG |
-
|
p.Lys250del |
Amino acid deletion |
Direct sequencing |
Wildin RS et al., 2002
|
Click here |
| 19 |
Deletion |
g.9333_9335delGGA |
c.750_752delGGA |
-
|
p.Glu251del |
Amino acid deletion |
PCR based assay |
Chatila TA et al., 2000
|
Click here |
| 20 |
Deletion |
g.9334_9336delGAG |
c.751_753delGAG |
-
|
p.Glu251del |
Amino acid deletion |
Direct sequencing |
Li B et al., 2007
|
Click here |
| 21 |
Deletion |
g.9334_9336delGAG |
c.751_753delGAG |
-
|
p.Glu251del |
Amino acid deletion |
Direct sequencing |
Gavin MA et al., 2006
|
Click here |
| 22 |
Deletion |
g.9334_9336delGAG |
c.751_753delGAG |
-
|
p.Glu251del |
Amino acid deletion |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 23 |
Substitution |
g.9403A>G |
c.816+4A>G |
-
|
- |
Splice donor defects |
PCR based assay |
Harbuz R et al., 2010
|
Click here |
| 24 |
Substitution |
g.9403A>G |
c.816+4A>G |
-
|
- |
Splice donor defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 25 |
Substitution |
g.9404G>A |
c.816+5G>A |
-
|
- |
Splice donor defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 26 |
Substitution |
g.11628T>C |
c.970T>C |
-
|
p.Phe324Leu |
Missense defects |
Direct sequencing |
Bacchetta R et al., 2006
|
Click here |
| 27 |
Substitution |
g.11628T>C |
c.970T>C |
-
|
p.Phe324Leu |
Missense defects |
Direct sequencing |
An YF et al., 2011
|
Click here |
| 28 |
Substitution |
g.11630C>T |
c.972C>T |
-
|
p.Phe324Leu |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 29 |
Substitution |
g.11668G>A |
c.1010G>A |
-
|
p.Arg337Gln |
Missense defects |
Direct sequencing |
Rubio-Cabezas O et al., 2009
|
Click here |
| 30 |
Substitution |
g.11673C>G |
c.1015C>G |
-
|
p.Pro339Ala |
Missense defects |
Southern blotting |
Rubio-Cabezas O et al., 2009
|
Click here |
| 31 |
Substitution |
g.11673C>G |
c.1015C>G |
-
|
p.Pro339Ala |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 32 |
Substitution |
g.11698G>A |
c.1040G>A |
-
|
p.Arg347His |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 33 |
Substitution |
g.11698G>A |
c.1040G>A |
-
|
p.Arg347His |
Missense defects |
Direct sequencing |
Wildin RS et al., 2002
|
Click here |
| 34 |
Substitution |
g.11706A>G |
c.1044+4A>G |
r.968_1044del
|
p.Glu323GlyfsX14 |
Splice donor defects, Exon skipping, Frameshift |
PCR based assay |
Chatila TA et al., 2000
|
Click here |
| 35 |
Insertion |
g.13098_19099insA |
c.1080_1081insA |
-
|
p.Asn361LysfsX2 |
Frameshift |
Direct sequencing |
An YF et al., 2011
|
Click here |
| 36 |
Substitution |
g.13105A>G |
c.1087A>G |
-
|
p.Ile363Val |
Missense defects |
Direct sequencing |
Kobayashi I et al., 2001
|
Click here |
| 37 |
Substitution |
g.13117T>C |
c.1099T>C |
-
|
p.Phe367Leu |
Missense defects |
Direct sequencing |
Suzuki S et al., 2007
|
Click here |
| 38 |
Substitution |
g.13119C>G |
c.1101C>G |
-
|
p.Phe367Leu |
Missense defects |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 39 |
Substitution |
g.13128G>A |
c.1110G>A |
-
|
p.Met370Ile |
Missense defects |
Direct sequencing, PCR based assay |
An YF et al., 2009
|
Click here |
| 40 |
Substitution |
g.13128G>A |
c.1110G>A |
-
|
p.Met370Ile |
Missense defects |
Direct sequencing |
An YF et al., 2011
|
Click here |
| 41 |
Substitution |
g.13131T>G |
c.1113T>G |
-
|
p.Phe371Leu |
Missense defects |
Direct sequencing |
Wildin RS et al., 2001
|
Click here |
| 42 |
Substitution |
g.13131T>G |
c.1113T>G |
-
|
p.Phe371Leu |
Missense defects |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 43 |
Deletion-Insertion |
g.13135_13136delTTinsGC |
c.1117_1118delTTinsGC |
-
|
p.Phe373Ala |
Missense defects |
Direct sequencing |
Bacchetta R et al., 2006
|
Click here |
| 44 |
Substitution |
g.13139T>G |
c.1121T>G |
-
|
p.Phe374Cys |
Missense defects |
Direct sequencing, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 45 |
Substitution |
g.13139T>G |
c.1121T>G |
-
|
p.Phe374Cys |
Missense defects |
Direct sequencing |
Halabi-Tawil M et al., 2009
|
Click here |
| 46 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Direct sequencing |
Wildin RS et al., 2001
|
Click here |
| 47 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Fluorescent sequencing |
Nieves DS et al., 2004
|
Click here |
| 48 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Direct sequencing |
Bennett CL et al., 2001
|
Click here |
| 49 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Dideoxy fingerprinting, PCR based assay |
Gambineri E et al., 2008
|
Click here |
| 50 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Direct sequencing |
Fuchizawa T et al., 2007
|
Click here |
| 51 |
Substitution |
g.13348G>A |
c.1150G>A |
-
|
p.Ala384Thr |
Missense defects |
Direct sequencing |
d'Hennezel E et al., 2009
|
Click here |
| 52 |
Substitution |
g.13387C>T |
c.1189C>T |
-
|
p.Arg397Trp |
Missense defects |
Direct sequencing |
Wildin RS et al., 2001
|
Click here |
| 53 |
Substitution |
g.13420G>A |
c.1222G>A |
-
|
p.Val408Met |
Missense defects |
Direct sequencing |
Rubio-Cabezas O et al., 2009
|
Click here |
| 54 |
Deletion |
g.13491_13492delCT |
c.1293_1294delCT |
-
|
p.X432ThrextX*26 |
Stop codon defects |
Direct sequencing |
Bennett CL et al., 2001
|
Click here |
|