Gene >> HRH3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340177 |
| Start |
62216478:62216478(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374571202
|
| CDS Mutation |
c.866C>T |
| AA Mutation |
p.Ala289Val(p.A289V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000340177 |
| Start |
62216494:62216494(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.850G>A |
| AA Mutation |
p.Ala284Thr(p.A284T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |