Primary Site >> Esophagus Cancer
Gene >> SST
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000287641 |
| Start |
187670279:187670279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.13C>T |
| AA Mutation |
p.Arg5Cys(p.R5C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |