| 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.2294G>A |
c.3G>A |
-
|
p.Met1? |
Start codon defects |
Direct sequencing |
Yue Z et al., 2010
|
Click here |
| 2 |
Insertion |
g.2631_2632insAGTCCAC |
c.340_341insAGTCCAC |
-
|
p.Arg114GlnfsX4 |
Frameshift |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 3 |
Substitution |
g.3868T>C |
c.836T>C |
-
|
p.Phe279Ser |
Missense defects |
Direct sequencing |
Lucke T et al., 2005
|
Click here |
| 4 |
Substitution |
g.3868T>C |
c.836T>C |
-
|
p.Phe279Ser |
Missense defects |
Direct sequencing |
Kilic SS et al., 2005
|
Click here |
| 5 |
Substitution |
g.7978C>T |
c.955C>T |
-
|
p.Gln319X |
Nonsense defects |
Direct sequencing |
Lou S et al., 2002
|
Click here |
| 6 |
Substitution |
g.8023C>T |
c.1000C>T |
-
|
p.Arg334X |
Nonsense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 7 |
Substitution |
g.11218A>G |
c.1097-2A>G |
r.1097_1147del
|
- |
Exon skipping |
Direct sequencing |
Dekel B et al., 2008
|
Click here |
| 8 |
Substitution |
g.11252G>C |
c.1129G>C |
-
|
p.Glu377Gln |
Missense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 9 |
Substitution |
g.11255G>T |
c.1132G>T |
-
|
p.Glu378X |
Nonsense defects |
Direct sequencing, PCR based assay |
Boerkoel CF et al., 2002
|
Click here |
| 10 |
Substitution |
g.11259A>C |
c.1136A>C |
-
|
p.His379Pro |
Missense defects |
Direct sequencing |
Kilic SS et al., 2005
|
Click here |
| 11 |
Deletion |
g.11269_11270delAA |
c.1146_1147delAA |
-
|
p.Leu382fs |
Frameshift |
Direct sequencing |
Taha D et al., 2004
|
Click here |
| 12 |
Deletion |
g.11269_11272delAAGT |
c.1146_1146+2delAAGT |
-
|
- |
Splice donor defects |
Direct sequencing |
Taha D et al., 2004
|
Click here |
| 13 |
Substitution |
g.20372G>C |
c.1402G>C |
-
|
p.Ala468Pro |
Missense defects |
Direct sequencing |
Sauerstein K et al., 2007
|
Click here |
| 14 |
Substitution |
g.20397G>A |
c.1427G>A |
-
|
p.Arg476Gln |
Missense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 15 |
Substitution |
g.20409C>T |
c.1439C>T |
-
|
p.Pro480Leu |
Missense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 16 |
Substitution |
g.26043C>T |
c.1681C>T |
-
|
p.Arg561Cys |
Missense defects |
Direct sequencing |
Bokenkamp A et al., 2005
|
Click here |
| 17 |
Substitution |
g.26044G>A |
c.1682G>A |
-
|
p.Arg561His |
Missense defects |
Direct sequencing |
Yue Z et al., 2010
|
Click here |
| 18 |
Substitution |
g.[26058A>T; 26060G>C] |
c.[1696A>T; 1698G>C] |
-
|
p.Met566Phe |
Missense defects |
Direct sequencing, PCR based assay |
Boerkoel CF et al., 2002
|
Click here |
| 19 |
Deletion |
g.26064delG |
c.1702delG |
-
|
p.Val568SerfsX1 |
Frameshift |
Direct sequencing, PCR based assay |
Boerkoel CF et al., 2002
|
Click here |
| 20 |
Substitution |
g.34650C>T |
c.1756C>T |
-
|
p.Arg586Trp |
Missense defects |
Direct sequencing, PCR based assay |
Boerkoel CF et al., 2002
|
Click here |
| 21 |
Deletion |
g.62874_62893delATCGATGGCTCCACCTCATC |
c.2263_2282delATCGATGGCTCCACCTCATC |
-
|
p.Ile755SerfsX2 |
Frameshift |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 22 |
Substitution |
g.62875T>G |
c.2264T>G |
-
|
p.Ile755Ser |
Missense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 23 |
Substitution |
g.64730T>G |
c.2462T>G |
-
|
p.Ile821Ser |
Missense defects |
Direct sequencing |
Clewing JM et al., 2007
|
Click here |
| 24 |
Substitution |
g.65803G>T |
c.2542G>T |
-
|
p.Glu848X |
Nonsense defects |
Direct sequencing |
Lucke T et al., 2005
|
Click here |
|