| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000403807 |
| Start |
22245059:22245059(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs763074545
|
| CDS Mutation |
c.160G>A |
| AA Mutation |
p.Val54Ile(p.V54I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000403807 |
| Start |
22245005:22245005(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.106A>G |
| AA Mutation |
p.Thr36Ala(p.T36A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> VPREB1
| Mutation ID |
1 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000403807 |
| Start |
22244945:22244945(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.47-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
|