Colon Cancer: Gene >> STOML2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000356493 |
| Start |
35101560:35101560(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.445G>A |
| AA Mutation |
p.Glu149Lys(p.E149K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356493 |
| Start |
35100960:35100960(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201944176
|
| CDS Mutation |
c.776G>A |
| AA Mutation |
p.Arg259Gln(p.R259Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> STOML2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356493 |
| Start |
35100051:35100051(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs767682475
|
| CDS Mutation |
c.1055G>A |
| AA Mutation |
p.Arg352Gln(p.R352Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000356493 |
| Start |
35101802:35101802(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs764083315
|
| CDS Mutation |
c.352G>A |
| AA Mutation |
p.Gly118Ser(p.G118S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000356493 |
| Start |
35102734:35102734(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.135G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|