Colon Cancer: Gene >> NHP2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274606 |
| Start |
178150989:178150989(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.235A>G |
| AA Mutation |
p.Met79Val(p.M79V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> NHP2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274606 |
| Start |
178149757:178149757(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.418G>A |
| AA Mutation |
p.Asp140Asn(p.D140N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000274606 |
| Start |
178153709:178153709(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs201390429
|
| CDS Mutation |
c.109C>T |
| AA Mutation |
p.Pro37Ser(p.P37S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|