Colon Cancer: Gene >> GIPR
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000590918 |
| Start |
45670635:45670635(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.73A>T |
| AA Mutation |
p.Thr25Ser(p.T25S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000590918 |
| Start |
45677954:45677954(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.973C>A |
| AA Mutation |
p.Leu325Met(p.L325M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> GIPR
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000590918 |
| Start |
45678188:45678188(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1114G>A |
| AA Mutation |
p.Ala372Thr(p.A372T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000590918 |
| Start |
45677751:45677751(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.896T>C |
| AA Mutation |
p.Ile299Thr(p.I299T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|