Colon Cancer: Gene >> PRSS22
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000161006 |
| Start |
2853941:2853941(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142215382
|
| CDS Mutation |
c.641G>A |
| AA Mutation |
p.Arg214Gln(p.R214Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000161006 |
| Start |
2853897:2853897(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.685G>T |
| AA Mutation |
p.Gly229Cys(p.G229C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> PRSS22
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000161006 |
| Start |
2853913:2853913(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.669G>T |
| AA Mutation |
p.Glu223Asp(p.E223D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|