Gene >> HRH4
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256906 |
| Start |
24477176:24477176(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.787T>C |
| AA Mutation |
p.Ser263Pro(p.S263P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256906 |
| Start |
24477480:24477480(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs149820026
|
| CDS Mutation |
c.1091G>A |
| AA Mutation |
p.Arg364His(p.R364H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |