Gene >> GPR37
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000303921 |
| Start |
124746731:124746731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1636C>G |
| AA Mutation |
p.Pro546Ala(p.P546A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000303921 |
| Start |
124764382:124764382(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.595A>T |
| AA Mutation |
p.Lys199Ter(p.K199*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |