Colon Cancer: Gene >> VPS26A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263559 |
| Start |
69168621:69168621(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.860T>C |
| AA Mutation |
p.Phe287Ser(p.F287S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000263559 |
| Start |
69171266:69171266(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140007940
|
| CDS Mutation |
c.981G>A |
| AA Mutation |
p.Met327Ile(p.M327I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> VPS26A
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000263559 |
| Start |
69155885:69155885(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.227T>G |
| AA Mutation |
p.Ile76Ser(p.I76S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000263559 |
| Start |
69157143:69157143(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs750841098
|
| CDS Mutation |
c.366C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
frameshift_variant |
| Transcription ID |
ENST00000263559 |
| Start |
69132954:69132955(version: GRCh38) |
| Mutation Type |
INS |
| dbSNP_RS |
null
|
| CDS Mutation |
c.64dupG |
| AA Mutation |
p.Glu22GlyfsTer11(p.E22Gfs*11) |
| Mutation Classification |
Frame_Shift_Ins |
| Feature Type |
Transcript |
|