Colon Cancer: Gene >> CHPT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229266 |
| Start |
101723822:101723822(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1040A>G |
| AA Mutation |
p.Glu347Gly(p.E347G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> CHPT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229266 |
| Start |
101726393:101726393(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1165G>A |
| AA Mutation |
p.Ala389Thr(p.A389T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000229266 |
| Start |
101723738:101723738(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.956A>G |
| AA Mutation |
p.Lys319Arg(p.K319R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|