Colon Cancer: Gene >> NANS
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000210444 |
| Start |
98078196:98078196(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs140402727
|
| CDS Mutation |
c.452G>A |
| AA Mutation |
p.Arg151His(p.R151H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> NANS
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000210444 |
| Start |
98077013:98077013(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.444A>C |
| AA Mutation |
p.Lys148Asn(p.K148N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000210444 |
| Start |
98083041:98083041(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1066A>C |
| AA Mutation |
p.Lys356Gln(p.K356Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000210444 |
| Start |
98078279:98078279(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.535T>C |
| AA Mutation |
p.Phe179Leu(p.F179L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|