| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263100 |
| Start |
58351520:58351520(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs770480372
|
| CDS Mutation |
c.781C>T |
| AA Mutation |
p.Arg261Cys(p.R261C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263100 |
| Start |
58353422:58353422(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.16G>A |
| AA Mutation |
p.Val6Ile(p.V6I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263100 |
| Start |
58353323:58353323(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.39C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |