Gene >> CRHR2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348438 |
| Start |
30699969:30699969(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.65G>A |
| AA Mutation |
p.Cys22Tyr(p.C22Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000471646 |
| Start |
30681971:30681971(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756090500
|
| CDS Mutation |
c.173C>A |
| AA Mutation |
p.Ala58Asp(p.A58D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |