| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156881562:156881562(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2311C>T |
| AA Mutation |
p.Arg771Cys(p.R771C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156879289:156879289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1973T>C |
| AA Mutation |
p.Val658Ala(p.V658A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000524377 |
| Start |
156881622:156881622(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2371T>A |
| AA Mutation |
p.Tyr791Asn(p.Y791N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |