| Mutation ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000054950 |
| Start |
32103478:32103478(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.886A>G |
| AA Mutation |
p.Lys296Glu(p.K296E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000054950 |
| Start |
32097237:32097237(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.348C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RCN1
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000054950 |
| Start |
32097249:32097249(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs141697360
|
| CDS Mutation |
c.360C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|