| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325980 |
| Start |
133240089:133240089(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.560C>T |
| AA Mutation |
p.Ala187Val(p.A187V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325980 |
| Start |
133240110:133240110(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.581C>T |
| AA Mutation |
p.Ala194Val(p.A194V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> VENTX
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325980 |
| Start |
133239717:133239717(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs776964051
|
| CDS Mutation |
c.283C>T |
| AA Mutation |
p.Arg95Cys(p.R95C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325980 |
| Start |
133239953:133239953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375001040
|
| CDS Mutation |
c.424C>T |
| AA Mutation |
p.Arg142Cys(p.R142C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|