Colon Cancer: Gene >> CLC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000221804 |
| Start |
39734329:39734329(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756972983
|
| CDS Mutation |
c.257G>A |
| AA Mutation |
p.Gly86Asp(p.G86D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000221804 |
| Start |
39734324:39734324(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.262G>T |
| AA Mutation |
p.Glu88Ter(p.E88*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CLC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000221804 |
| Start |
39731424:39731424(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368189111
|
| CDS Mutation |
c.385G>T |
| AA Mutation |
p.Asp129Tyr(p.D129Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|