| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98732544:98732544(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3725A>G |
| AA Mutation |
p.Tyr1242Cys(p.Y1242C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98671552:98671552(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1626G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000551964 |
| Start |
98715459:98715459(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.2991G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |