Primary Site >> Esophagus Cancer
Gene >> GRP
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000256857 |
| Start |
59225497:59225497(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.145T>G |
| AA Mutation |
p.Leu49Val(p.L49V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |