Colon Cancer: Gene >> IRGM
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000522154 |
| Start |
150848395:150848395(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.272T>A |
| AA Mutation |
p.Leu91Gln(p.L91Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000522154 |
| Start |
150848188:150848188(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.65T>C |
| AA Mutation |
p.Ile22Thr(p.I22T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> IRGM
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000522154 |
| Start |
150848523:150848523(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.400G>A |
| AA Mutation |
p.Ala134Thr(p.A134T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000522154 |
| Start |
150848344:150848344(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.221G>T |
| AA Mutation |
p.Arg74Ile(p.R74I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|