Gene >> RHCG
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268122 |
| Start |
89477938:89477938(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.874G>A |
| AA Mutation |
p.Ala292Thr(p.A292T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268122 |
| Start |
89483132:89483132(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.457A>G |
| AA Mutation |
p.Ile153Val(p.I153V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |