| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349496 |
| Start |
41224622:41224622(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121913403
|
| CDS Mutation |
c.110C>T |
| AA Mutation |
p.Ser37Phe(p.S37F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349496 |
| Start |
41225119:41225119(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.407T>C |
| AA Mutation |
p.Val136Ala(p.V136A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000349496 |
| Start |
41224609:41224609(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.97T>G |
| AA Mutation |
p.Ser33Ala(p.S33A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |