| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368474 |
| Start |
154590279:154590279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs748161184
|
| CDS Mutation |
c.2401C>T |
| AA Mutation |
p.Arg801Cys(p.R801C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368474 |
| Start |
154602313:154602313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.329A>G |
| AA Mutation |
p.His110Arg(p.H110R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368474 |
| Start |
154585825:154585825(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3243C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |