Colon Cancer: Gene >> FAM98B
No Mutation Annotation! |
Rectum Cancer: Gene >> FAM98B
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000491535 |
| Start |
38470273:38470273(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.399G>T |
| AA Mutation |
p.Lys133Asn(p.K133N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000491535 |
| Start |
38481357:38481357(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs761793572
|
| CDS Mutation |
c.795G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000491535 |
| Start |
38473579:38473579(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.606A>G |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
stop_gained |
| Transcription ID |
ENST00000491535 |
| Start |
38464142:38464142(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.182C>A |
| AA Mutation |
p.Ser61Ter(p.S61*) |
| Mutation Classification |
Nonsense_Mutation |
| Feature Type |
Transcript |
|