Gene >> RHAG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371175 |
| Start |
49615737:49615737(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.527C>A |
| AA Mutation |
p.Ala176Asp(p.A176D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371175 |
| Start |
49636676:49636676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.137T>C |
| AA Mutation |
p.Ile46Thr(p.I46T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |