| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222002 |
| Start |
47883599:47883599(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.323C>A |
| AA Mutation |
p.Ser108Tyr(p.S108Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222002 |
| Start |
47882143:47882143(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.413A>C |
| AA Mutation |
p.Lys138Thr(p.K138T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SULT2A1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000222002 |
| Start |
47882133:47882133(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.423G>T |
| AA Mutation |
p.Lys141Asn(p.K141N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|