| Sl.No |
Mutation type |
Genomic level change |
CDS level change |
RNA level change |
Protein level change |
Mutation effects |
Expt. name |
PubMed |
Mutation viewer |
| 1 |
Insertion |
g.36620_36621insG |
c.117_118insG |
-
|
p.Ala40fs |
Frameshift |
PCR based assay |
Barbosa MD et al., 1996
|
Click here |
| 2 |
Duplications |
g.36621dupG |
c.118dupG |
r.118dupg
|
p.Ala40GlyfsX24 |
Frameshift |
Direct sequencing |
Nagle DL et al., 1996
|
Click here |
| 3 |
Substitution |
g.36651C>T |
c.148C>T |
-
|
p.Arg50X |
Nonsense defects |
Direct sequencing, SSCP |
Barbosa MD et al., 1997
|
Click here |
| 4 |
Insertion |
g.56678insT |
c.575insT |
-
|
p.Leu192PhefsX6 |
Frameshift |
Direct sequencing |
Scherber E et al., 2009
|
Click here |
| 5 |
Deletion |
g.57570delG |
c.1467delG |
-
|
p.Glu489AspfsX78 |
Frameshift |
Direct sequencing |
Nagle DL et al., 1996
|
Click here |
| 6 |
Substitution |
g.57643C>T |
c.1540C>T |
-
|
p.Arg514X |
Nonsense defects |
Direct sequencing |
Zarzour W et al., 2005
|
Click here |
| 7 |
Deletion |
g.58005delA |
c.1902delA |
-
|
p.Ala635GlnfsX13 |
Frameshift |
Direct sequencing, SSCP |
Karim MA et al., 1997
|
Click here |
| 8 |
Deletion |
g.60198delG |
c.2413delG |
-
|
p.Glu805X |
Nonsense defects |
NA |
Westbroek W et al., 2007
|
Click here |
| 9 |
Deletion |
g.60239delA |
c.2454delA |
-
|
p.Ala819HisfsX5 |
Frameshift |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 10 |
Deletion |
g.60405delT |
c.2620delT |
-
|
p.Tyr875MetfsX61 |
Frameshift |
Direct sequencing |
Certain S et al., 2000
|
Click here |
| 11 |
Deletion |
g.60405delT |
c.2620delT |
-
|
p.Tyr875MetfsX24 |
Frameshift |
Direct sequencing |
Dufourcq-Lagelouse R et al., 1999
|
Click here |
| 12 |
Deletion |
g.60858_60859delAA |
c.3073_3074delAA |
-
|
p.Asn1025GlnfsX6 |
Frameshift |
Direct sequencing, SSCP |
Barbosa MD et al., 1997
|
Click here |
| 13 |
Substitution |
g.60870C>T |
c.3085C>T |
-
|
p.Gln1029X |
Nonsense defects |
Direct sequencing, SSCP |
Barbosa MD et al., 1997
|
Click here |
| 14 |
Substitution |
g.61095C>T |
c.3310C>T |
-
|
p.Arg1104X |
Nonsense defects |
Direct sequencing |
Certain S et al., 2000
|
Click here |
| 15 |
Substitution |
g.61095C>T |
c.3310C>T |
-
|
p.Arg1104X |
Nonsense defects |
PCR based assay |
Nagle DL et al., 1996
|
Click here |
| 16 |
Duplications |
g.62296dupA |
c.3434dupA |
-
|
p.His1145GlnfsX9 |
Frameshift |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 17 |
Substitution |
g.63923C>T |
c.3622C>T |
-
|
p.Gln1208X |
Nonsense defects |
Direct sequencing |
Morrone K et al., 2010
|
Click here |
| 18 |
Substitution |
g.73354C>G |
c.4052C>G |
-
|
p.Ser1351X |
Nonsense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 19 |
Deletion |
g.74953delT |
c.4274delT |
-
|
p.Leu1425TyrfsX2 |
Frameshift |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 20 |
Substitution |
g.75040C>A |
c.4361C>A |
-
|
p.Ala1454Asp |
Missense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 21 |
Substitution |
g.78220G>A |
c.4688G>A |
-
|
p.Arg1563His |
Missense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 22 |
Deletion |
g.84975delA |
c.5004delA |
-
|
p.Gly1668fs |
Frameshift |
Direct sequencing |
Scherber E et al., 2009
|
Click here |
| 23 |
Substitution |
g.85903T>A |
c.5061T>A |
-
|
p.Tyr1687X |
Nonsense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 24 |
Deletion |
g.89715delA |
c.5317delA |
-
|
p.Arg1773AspfsX13 |
Frameshift |
Direct sequencing |
Certain S et al., 2000
|
Click here |
| 25 |
Substitution |
g.91880C>T |
c.5506C>T |
-
|
p.Arg1836X |
Nonsense defects |
Direct sequencing |
Kaya Z et al., 2011
|
Click here |
| 26 |
Deletion |
g.91893delC |
c.5519delC |
-
|
p.Ser1840fs |
Frameshift |
Direct sequencing |
Scherber E et al., 2009
|
Click here |
| 27 |
Substitution |
g.100717T>A |
c.5996T>A |
-
|
p.Val1999Asp |
Missense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 28 |
Substitution |
g.100799C>A |
c.6078C>A |
-
|
p.Tyr2026X |
Nonsense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 29 |
Deletion |
g.114844delT |
c.7555delT |
-
|
p.Tyr2519IlefsX10 |
Frameshift |
Direct sequencing |
Certain S et al., 2000
|
Click here |
| 30 |
Substitution |
g.132331G>A |
c.8428G>A |
-
|
p.Glu2810Lys |
Missense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 31 |
Substitution |
g.133062G>A |
c.8583G>A |
-
|
p.Trp2861X |
Nonsense defects |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 32 |
Deletion |
g.150172delA |
c.9590delA |
-
|
p.Tyr3197LeufsX90 |
Frameshift |
Direct sequencing |
Certain S et al., 2000
|
Click here |
| 33 |
Deletion |
g.150172delA |
c.9590delA |
-
|
p.Tyr3197LeufsX90 |
Frameshift |
Direct sequencing, SSCP |
Karim MA et al., 1997
|
Click here |
| 34 |
Deletion |
g.150172delA |
c.9590delA |
-
|
p.Tyr3197LeufsX90 |
Frameshift |
Direct sequencing |
Scherber E et al., 2009
|
Click here |
| 35 |
Deletion |
g.154832delT |
c.9893delT |
-
|
p.Phe3298SerfsX7 |
Frameshift |
Direct sequencing |
Zarzour W et al., 2005
|
Click here |
| 36 |
Substitution |
g.157814A>G |
c.10127A>G |
-
|
p.Asn3376Ser |
Missense defects |
NA |
Westbroek W et al., 2007
|
Click here |
| 37 |
Deletion |
g.169669delA |
c.10395delA |
-
|
p.Gly3466AlafsX2 |
Frameshift |
Direct sequencing, Heteroduplex analysis, SSCP |
Karim MA et al., 2002
|
Click here |
| 38 |
Substitution |
g.189794G>T |
c.11002G>T |
-
|
p.Glu3668X |
Nonsense defects |
Direct sequencing |
Morrone K et al., 2010
|
Click here |
|