Colon Cancer: Gene >> TGFA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295400 |
| Start |
70465725:70465725(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs147786817
|
| CDS Mutation |
c.106G>A |
| AA Mutation |
p.Val36Met(p.V36M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> TGFA
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295400 |
| Start |
70456369:70456369(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.335C>T |
| AA Mutation |
p.Ala112Val(p.A112V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|