| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335209 |
| Start |
117049118:117049118(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.250A>G |
| AA Mutation |
p.Asn84Asp(p.N84D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000335209 |
| Start |
117041977:117041977(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs765292467
|
| CDS Mutation |
c.537C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TESC
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000335209 |
| Start |
117056813:117056813(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.202G>A |
| AA Mutation |
p.Asp68Asn(p.D68N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|