Primary Site >> Liver Cancer
Gene >> HMGB2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296503 |
| Start |
173332085:173332085(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.625G>A |
| AA Mutation |
p.Glu209Lys(p.E209K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |