Colon Cancer: Gene >> RAP1A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356415 |
| Start |
111704362:111704362(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.344G>A |
| AA Mutation |
p.Gly115Asp(p.G115D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356415 |
| Start |
111691385:111691385(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.25C>A |
| AA Mutation |
p.Leu9Ile(p.L9I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RAP1A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356415 |
| Start |
111697474:111697474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.160G>A |
| AA Mutation |
p.Glu54Lys(p.E54K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356415 |
| Start |
111703399:111703399(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.247T>G |
| AA Mutation |
p.Ser83Ala(p.S83A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|