Colon Cancer: Gene >> CHAC2
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000295304 |
| Start |
53767952:53767952(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.66C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> CHAC2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295304 |
| Start |
53774496:53774496(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.526G>C |
| AA Mutation |
p.Glu176Gln(p.E176Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000295304 |
| Start |
53774434:53774434(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.464T>G |
| AA Mutation |
p.Leu155Arg(p.L155R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|