Colon Cancer: Gene >> RPS6
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380394 |
| Start |
19376574:19376574(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs756253114
|
| CDS Mutation |
c.574A>G |
| AA Mutation |
p.Ile192Val(p.I192V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380394 |
| Start |
19376577:19376577(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.571C>T |
| AA Mutation |
p.Arg191Cys(p.R191C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> RPS6
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380394 |
| Start |
19376545:19376545(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.603A>C |
| AA Mutation |
p.Lys201Asn(p.K201N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000380394 |
| Start |
19378484:19378484(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs778272571
|
| CDS Mutation |
c.380C>A |
| AA Mutation |
p.Thr127Asn(p.T127N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|