Primary Site >> Stomach Cancer
Gene >> UCN
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296099 |
| Start |
27307564:27307564(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.332G>A |
| AA Mutation |
p.Arg111His(p.R111H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |