Colon Cancer: Gene >> CMTM2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268595 |
| Start |
66587019:66587019(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.467C>A |
| AA Mutation |
p.Ala156Asp(p.A156D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268595 |
| Start |
66580116:66580116(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs368740252
|
| CDS Mutation |
c.376A>G |
| AA Mutation |
p.Ser126Gly(p.S126G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> CMTM2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268595 |
| Start |
66579630:66579630(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.23G>A |
| AA Mutation |
p.Gly8Glu(p.G8E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000268595 |
| Start |
66587078:66587078(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.526C>A |
| AA Mutation |
p.Leu176Ile(p.L176I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|