| Mutation ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000348227 |
| Start |
74425097:74425097(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.658C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
5 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000348227 |
| Start |
74424898:74424898(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374027089
|
| CDS Mutation |
c.558G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> WDR54
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000348227 |
| Start |
74423325:74423325(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs754183319
|
| CDS Mutation |
c.292G>A |
| AA Mutation |
p.Glu98Lys(p.E98K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|