Primary Site >> Liver Cancer
Gene >> AMH
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000221496 |
| Start |
2249688:2249688(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.356G>T |
| AA Mutation |
p.Gly119Val(p.G119V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |