Colon Cancer: Gene >> SNUPN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308588 |
| Start |
75609931:75609931(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs377184433
|
| CDS Mutation |
c.367G>A |
| AA Mutation |
p.Val123Met(p.V123M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000308588 |
| Start |
75609640:75609640(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.420T>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> SNUPN
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308588 |
| Start |
75598519:75598519(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.922C>A |
| AA Mutation |
p.Gln308Lys(p.Q308K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000308588 |
| Start |
75601179:75601179(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs142962123
|
| CDS Mutation |
c.718G>A |
| AA Mutation |
p.Glu240Lys(p.E240K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|