Colon Cancer: Gene >> FITM2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000396825 |
| Start |
44306927:44306927(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs370245406
|
| CDS Mutation |
c.487G>A |
| AA Mutation |
p.Ala163Thr(p.A163T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000396825 |
| Start |
44307161:44307161(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs771219892
|
| CDS Mutation |
c.253G>A |
| AA Mutation |
p.Gly85Ser(p.G85S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> FITM2
No Mutation Annotation! |