Colon Cancer: Gene >> EXOSC4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316052 |
| Start |
144080453:144080453(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs376508817
|
| CDS Mutation |
c.590C>T |
| AA Mutation |
p.Ala197Val(p.A197V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316052 |
| Start |
144080474:144080474(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs373942429
|
| CDS Mutation |
c.611G>A |
| AA Mutation |
p.Arg204Gln(p.R204Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> EXOSC4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316052 |
| Start |
144080082:144080082(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201630396
|
| CDS Mutation |
c.311G>A |
| AA Mutation |
p.Arg104His(p.R104H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000316052 |
| Start |
144080339:144080339(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145830532
|
| CDS Mutation |
c.476C>T |
| AA Mutation |
p.Ala159Val(p.A159V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|