| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98677490:98677490(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1859A>G |
| AA Mutation |
p.His620Arg(p.H620R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98727309:98727309(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3593A>G |
| AA Mutation |
p.Tyr1198Cys(p.Y1198C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98723236:98723236(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.3128A>G |
| AA Mutation |
p.His1043Arg(p.H1043R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |