Primary Site >> Stomach Cancer
Gene >> HMGA1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000311487 |
| Start |
34242748:34242748(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.172C>T |
| AA Mutation |
p.Arg58Trp(p.R58W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |