| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361842 |
| Start |
6770788:6770788(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.653A>G |
| AA Mutation |
p.Asn218Ser(p.N218S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361842 |
| Start |
6758142:6758142(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs762291469
|
| CDS Mutation |
c.86G>A |
| AA Mutation |
p.Arg29Gln(p.R29Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> XAF1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000361842 |
| Start |
6756106:6756106(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.28A>T |
| AA Mutation |
p.Asn10Tyr(p.N10Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|