| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000520429 |
| Start |
99550290:99550290(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.458A>G |
| AA Mutation |
p.Tyr153Cys(p.Y153C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000520429 |
| Start |
99561393:99561393(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.268T>C |
| AA Mutation |
p.Cys90Arg(p.C90R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CCNC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000520429 |
| Start |
99562907:99562907(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs755107219
|
| CDS Mutation |
c.74G>A |
| AA Mutation |
p.Arg25His(p.R25H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|