Colon Cancer: Gene >> AP5M1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261558 |
| Start |
57274320:57274320(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.151T>A |
| AA Mutation |
p.Phe51Ile(p.F51I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000261558 |
| Start |
57274373:57274373(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148346858
|
| CDS Mutation |
c.204C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> AP5M1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261558 |
| Start |
57280292:57280292(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.818C>A |
| AA Mutation |
p.Thr273Asn(p.T273N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261558 |
| Start |
57269383:57269383(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.69C>A |
| AA Mutation |
p.Phe23Leu(p.F23L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000261558 |
| Start |
57274731:57274731(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.562T>C |
| AA Mutation |
p.Ser188Pro(p.S188P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|