Colon Cancer: Gene >> RRAD
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299759 |
| Start |
66923593:66923593(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs757648876
|
| CDS Mutation |
c.572G>A |
| AA Mutation |
p.Arg191Gln(p.R191Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299759 |
| Start |
66922164:66922164(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.839G>A |
| AA Mutation |
p.Arg280His(p.R280H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RRAD
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299759 |
| Start |
66922117:66922117(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764593765
|
| CDS Mutation |
c.886C>T |
| AA Mutation |
p.Arg296Cys(p.R296C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000299759 |
| Start |
66922197:66922197(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.806G>A |
| AA Mutation |
p.Arg269Gln(p.R269Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|