| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328945 |
| Start |
81999543:81999543(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs572262577
|
| CDS Mutation |
c.750G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000328945 |
| Start |
81999231:81999231(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1062T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SDR42E1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000328945 |
| Start |
81999324:81999324(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.969T>G |
| AA Mutation |
p.His323Gln(p.H323Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|