| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354968 |
| Start |
47221787:47221787(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374127769
|
| CDS Mutation |
c.419G>A |
| AA Mutation |
p.Arg140His(p.R140H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000354968 |
| Start |
47221782:47221782(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs13589
|
| CDS Mutation |
c.414C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> MYL4
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000354968 |
| Start |
47221774:47221774(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs375241929
|
| CDS Mutation |
c.406G>A |
| AA Mutation |
p.Val136Met(p.V136M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|