| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292782 |
| Start |
182963977:182963977(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.293C>T |
| AA Mutation |
p.Ala98Val(p.A98V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292782 |
| Start |
182965690:182965690(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.67G>A |
| AA Mutation |
p.Glu23Lys(p.E23K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> DCUN1D1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292782 |
| Start |
182965720:182965720(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.37C>T |
| AA Mutation |
p.Arg13Cys(p.R13C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000292782 |
| Start |
182965568:182965568(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.189G>T |
| AA Mutation |
p.Lys63Asn(p.K63N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|