Gene >> HCK
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000534862 |
| Start |
32093900:32093900(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1130A>G |
| AA Mutation |
p.Tyr377Cys(p.Y377C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000534862 |
| Start |
32074698:32074698(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.405C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |