| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000497571 |
| Start |
3782048:3782048(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.269T>A |
| AA Mutation |
p.Leu90His(p.L90H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000497571 |
| Start |
3780141:3780141(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.765C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> KLF6
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000497571 |
| Start |
3782085:3782085(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs753610916
|
| CDS Mutation |
c.232G>A |
| AA Mutation |
p.Glu78Lys(p.E78K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000497571 |
| Start |
3781925:3781925(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.392G>A |
| AA Mutation |
p.Gly131Asp(p.G131D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|