Gene >> OR4C6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314259 |
| Start |
55665530:55665530(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs367948844
|
| CDS Mutation |
c.364G>A |
| AA Mutation |
p.Val122Met(p.V122M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000314259 |
| Start |
55665935:55665935(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs749468804
|
| CDS Mutation |
c.769A>G |
| AA Mutation |
p.Met257Val(p.M257V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |