| 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.556C>T |
c.117+59C>T |
-
|
- |
Splice anomalies |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 2 |
Substitution |
g.891C>T |
c.117+394C>T |
-
|
- |
Splice anomalies |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 3 |
Substitution |
g.1022G>T |
c.117+525G>T |
-
|
- |
Splice anomalies |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 4 |
Substitution |
g.1473G>A |
c.175G>A |
-
|
p.Ala59Thr |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 5 |
Deletion |
g.1475_1476delAC |
c.177_178delAC |
-
|
p.Tyr61HisfsX10 |
Frameshift |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 6 |
Deletion |
g.1512delC |
c.214delC |
-
|
p.Asn73ThrfsX3 |
Frameshift |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 7 |
Deletion |
g.1512delC |
c.214delC |
-
|
p.Asn73ThrfsX3 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 8 |
Substitution |
g.1545C>T |
c.247C>T |
-
|
p.Arg83X |
Nonsense defects |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 9 |
Substitution |
g.1545C>T |
c.247C>T |
-
|
p.Arg83X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 10 |
Substitution |
g.1675C>T |
c.292C>T |
-
|
p.Gln98X |
Nonsense defects |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 11 |
Substitution |
g.1794G>A |
c.322-1G>A |
r.322_388del
|
p.Lys108_Ser129delfsX15 |
Splice acceptor defects, Exon skipping, Frameshift |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 12 |
Insertion |
g.2119insC |
c.403insC |
-
|
p.Tyr135LeufsX7 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 13 |
Substitution |
g.2135T>C |
c.419T>C |
-
|
p.Ile140Thr |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 14 |
Deletion |
g.2157delA |
c.441delA |
-
|
p.Gly149AlafsX13 |
Frameshift |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 15 |
Deletion |
g.2157delA |
c.441delA |
-
|
p.Gly149AlafsX13 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 16 |
Deletion |
g.2248delC |
c.532delC |
-
|
p.Gln178ArgfsX71 |
Frameshift |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 17 |
Deletion |
g.2248delC |
c.532delC |
-
|
p.Gln178ArgfsX71 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 18 |
Substitution |
g.2290G>A |
c.569+5G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 19 |
Substitution |
g.3757A>G |
c.610A>G |
-
|
p.Met204Val |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 20 |
Deletion |
g.3900delT |
c.627delT |
-
|
p.Val210TrpfsX39 |
Frameshift |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 21 |
Deletion |
g.3900delT |
c.627delT |
-
|
p.Val210TrpfsX39 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 22 |
Substitution |
g.3913C>T |
c.640C>T |
-
|
p.Arg214X |
Nonsense defects |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 23 |
Substitution |
g.3913C>T |
c.640C>T |
-
|
p.Arg214X |
Nonsense defects |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 24 |
Substitution |
g.3913C>T |
c.640C>T |
-
|
p.Arg214X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 25 |
Substitution |
g.4212G>T |
c.753+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 26 |
Substitution |
g.4212G>T |
c.753+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 27 |
Substitution |
g.4212G>T |
c.753+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 28 |
Substitution |
g.4212G>T |
c.753+1G>T |
-
|
- |
Splice donor defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 29 |
Substitution |
g.4214G>A |
c.753+3G>A |
-
|
- |
Splice donor defects |
NA |
Hazen MM et al., 2008
|
Click here |
| 30 |
Substitution |
g.4388G>C |
c.754-1G>C |
-
|
p.Asp252fsX89 |
Splice acceptor defects, Frameshift |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 31 |
Substitution |
g.4388G>C |
c.754-1G>C |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 32 |
Substitution |
g.4401C>T |
c.766C>T |
-
|
p.Arg256X |
Nonsense defects |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 33 |
Substitution |
g.4401C>T |
c.766C>T |
-
|
p.Arg256X |
Nonsense defects |
Direct sequencing |
Zhizhuo H et al., 2012
|
Click here |
| 34 |
Substitution |
g.4452C>T |
c.817C>T |
-
|
p.Arg273X |
Nonsense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 35 |
Substitution |
g.4452C>T |
c.817C>T |
-
|
p.Arg273X |
Nonsense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 36 |
Substitution |
g.4452C>T |
c.817C>T |
-
|
p.Arg273X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 37 |
Substitution |
g.4618C>T |
c.869C>T |
-
|
p.Ser290Leu |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 38 |
Substitution |
g.4775G>A |
c.952-1G>A |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 39 |
Substitution |
g.4775G>A |
c.952-1G>A |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 40 |
Substitution |
g.4880G>A |
c.1055+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 41 |
Substitution |
g.7889G>A |
c.1145G>A |
-
|
p.Trp382X |
Nonsense defects |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 42 |
Substitution |
g.7889G>A |
c.1145G>A |
-
|
p.Trp382X |
Nonsense defects |
Direct sequencing |
Bryceson YT et al., 2007
|
Click here |
| 43 |
Substitution |
g.7889G>A |
c.1145G>A |
-
|
p.Trp382X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 44 |
Substitution |
g.8041C>T |
c.1193C>T |
-
|
p.Ser398Leu |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 45 |
Substitution |
g.8056T>C |
c.1208T>C |
-
|
p.Leu403Pro |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 46 |
Substitution |
g.8056T>C |
c.1208T>C |
-
|
p.Leu403Pro |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 47 |
Substitution |
g.8063C>G |
c.1215C>G |
-
|
p.Tyr405X |
Nonsense defects |
Direct sequencing |
Zhizhuo H et al., 2012
|
Click here |
| 48 |
Deletion |
g.8073delC |
c.1225delC |
-
|
p.Leu409SerfsX33 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 49 |
Substitution |
g.8089G>T |
c.1241G>T |
-
|
p.Arg414Leu |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 50 |
Substitution |
g.8377C>T |
c.1387C>T |
-
|
p.Gln463X |
Nonsense defects |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 51 |
Substitution |
g.8377C>T |
c.1387C>T |
-
|
p.Gln463X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 52 |
Substitution |
g.8380G>A |
c.1389+1G>A |
-
|
p.Thr464fs |
Splice donor defects, Frameshift |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 53 |
Substitution |
g.8380G>A |
c.1389+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 54 |
Substitution |
g.8380G>A |
c.1389+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 55 |
Substitution |
g.8811G>T |
c.1545-1G>T |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 56 |
Substitution |
g.8846C>T |
c.1579C>T |
-
|
p.Arg527Trp |
Missense defects |
NA |
Hazen MM et al., 2008
|
Click here |
| 57 |
Substitution |
g.8864G>C |
c.1596+1G>C |
r.1596_1597ins77
|
p.Val533fsX41 |
Splice donor defects, Exon skipping, Frameshift |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 58 |
Substitution |
g.8864G>C |
c.1596+1G>C |
r.1545_1596del
|
p.Asn515_Leu532delfsX16 |
Splice donor defects, Exon skipping, Amino acid deletion, Frameshift |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 59 |
Substitution |
g.8864G>C |
c.1596+1G>C |
-
|
p.Val533TrpfsX41 |
Splice donor defects, Frameshift |
Direct sequencing |
Zhizhuo H et al., 2012
|
Click here |
| 60 |
Deletion |
g.9037delG |
c.1693delG |
-
|
p.Glu565SerfsX7 |
Frameshift |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 61 |
Duplications |
g.9067dupA |
c.1723dupA |
-
|
p.Glu575fs |
Frameshift |
Direct sequencing |
Yamamoto K et al., 2004
|
Click here |
| 62 |
Insertion |
g.9215_9216insT |
c.1754_1755insT |
-
|
p.His586fs |
Frameshift |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 63 |
Substitution |
g.9221G>A |
c.1760G>A |
-
|
p.Arg587His |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 64 |
Substitution |
g.9281G>C |
c.1820G>C |
-
|
p.Arg607Pro |
Missense defects |
Direct sequencing |
Rohr J et al., 2010
|
Click here |
| 65 |
Deletion |
g.9283_9294del12 |
c.1822_1833del12 |
-
|
p.Val608_Ala611del |
Amino acid deletion |
Direct sequencing |
Feldmann J et al., 2003
|
Click here |
| 66 |
Deletion |
g.9283_9294del12 |
c.1822_1833del12 |
-
|
p.Val608_Ala611del |
Amino acid deletion |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 67 |
Deletion |
g.9283_9294del12 |
c.1822_1833del12 |
-
|
p.Val608_Ala611del |
Amino acid deletion |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 68 |
Substitution |
g.9308A>G |
c.1847A>G |
-
|
p.Glu616Gly |
Splice anomalies |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 69 |
Substitution |
g.9308A>G |
c.1847A>G |
-
|
p.Glu616Gly |
Missense defects |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 70 |
Substitution |
g.9308A>G |
c.1847A>G |
-
|
p.Glu616Gly |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 71 |
Substitution |
g.9746T>C |
c.1940T>C |
-
|
p.Leu647Pro |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 72 |
Substitution |
g.10000A>G |
c.1993-2A>G |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 73 |
Substitution |
g.10048G>C |
c.2039G>C |
-
|
p.Arg680Pro |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 74 |
Substitution |
g.10048G>C |
c.2039G>C |
-
|
p.Arg680Pro |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 75 |
Substitution |
g.10066C>A |
c.2057C>A |
-
|
p.Ser686X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 76 |
Substitution |
g.10275G>A |
c.2180G>A |
-
|
p.Arg727Gln |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 77 |
Substitution |
g.10286G>A |
c.2191G>A |
-
|
p.Val731Met |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 78 |
Substitution |
g.10307C>T |
c.2212C>T |
-
|
p.Gln738X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 79 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 80 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 81 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 82 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 83 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
Direct sequencing |
Rohr J et al., 2010
|
Click here |
| 84 |
Deletion |
g.10622_10625delGGAG |
c.2346_2349delGGAG |
-
|
p.Arg782SerfsX12 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 85 |
Substitution |
g.10644G>A |
c.2367+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 86 |
Substitution |
g.11671A>G |
c.2368-2A>G |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Rohr J et al., 2010
|
Click here |
| 87 |
Deletion |
g.11686delT |
c.2381delT |
-
|
p.Leu794ArgfsX2 |
Frameshift |
Direct sequencing |
Meeths M et al., 2011
|
Click here |
| 88 |
Deletion-Insertion |
g.11742_11744delAACinsT |
c.2437_2439delAACinsT |
-
|
p.Asn813PhefsX47 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 89 |
Deletion |
g.13399_13402delTCAC |
c.2477_2480delTCAC |
-
|
p.Leu826GlnfsX20 |
Frameshift |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 90 |
Substitution |
g.13565T>G |
c.2570T>G |
-
|
p.Phe857Cys |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 91 |
Substitution |
g.13570G>A |
c.2575G>A |
-
|
p.Ala859Thr |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 92 |
Substitution |
g.14056G>A |
c.2626-1G>A |
-
|
- |
Splice acceptor defects |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 93 |
Substitution |
g.14056G>A |
c.2626-1G>A |
-
|
- |
Splice acceptor defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 94 |
Substitution |
g.14073T>C |
c.2642T>C |
-
|
p.Leu881Pro |
Missense defects |
Direct sequencing |
Meeths M et al., 2011
|
Click here |
| 95 |
Substitution |
g.14081C>T |
c.2650C>T |
-
|
p.Gln884X |
Nonsense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 96 |
Substitution |
g.14103T>C |
c.2672T>C |
-
|
p.Leu891Pro |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 97 |
Substitution |
g.14141G>A |
c.2709+1G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Zhizhuo H et al., 2012
|
Click here |
| 98 |
Substitution |
g.14308C>T |
c.2782C>T |
-
|
p.Arg928Cys |
Missense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 99 |
Substitution |
g.14309G>C |
c.2783G>C |
-
|
p.Arg928Pro |
Missense defects |
PCR based assay |
Rudd E et al., 2008
|
Click here |
| 100 |
Substitution |
g.14309G>C |
c.2783G>C |
-
|
p.Arg928Pro |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 101 |
Substitution |
g.14695G>A |
c.2954+5G>A |
-
|
- |
Splice donor defects |
Direct sequencing |
Yoon HS et al., 2009
|
Click here |
| 102 |
Deletion |
g.15121delA |
c.2954+431delA |
r.2955_3151del
|
- |
Splice anomalies, Exon skipping |
Direct sequencing |
Santoro A et al., 2008
|
Click here |
| 103 |
Substitution |
g.15829G>A |
c.3049G>A |
-
|
p.Glu1017Lys |
Missense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 104 |
Deletion |
g.15862delC |
c.3082delC |
-
|
p.Leu1028X |
Nonsense defects |
Direct sequencing |
Santoro A et al., 2006
|
Click here |
| 105 |
Deletion |
g.15862delC |
c.3082delC |
-
|
p.Leu1028X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 106 |
Substitution |
g.15911T>G |
c.3131T>G |
-
|
p.Leu1044Arg |
Missense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 107 |
Substitution |
g.16673C>T |
c.3193C>T |
-
|
p.Arg1065X |
Nonsense defects |
Direct sequencing |
Zur Stadt U et al., 2006
|
Click here |
| 108 |
Substitution |
g.16673C>T |
c.3193C>T |
-
|
p.Arg1065X |
Nonsense defects |
Direct sequencing |
Sieni E et al., 2011
|
Click here |
| 109 |
Duplications |
g.16706dupG |
c.3226dupG |
-
|
p.His1076fs |
Frameshift |
Direct sequencing |
Santoro A et al., 2006
|
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|