| Mutation ID |
6 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000269582 |
| Start |
39670161:39670162(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
rs771451039
|
| CDS Mutation |
c.627dupG |
| AA Mutation |
p.His210AlafsTer27(p.H210Afs*27) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
| Mutation ID |
7 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000269582 |
| Start |
39669628:39669628(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.203-1G>A |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PNMT
No Mutation Annotation! |