Colon Cancer: Gene >> TYROBP
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000262629 |
| Start |
35907527:35907527(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.148G>T |
| AA Mutation |
p.Asp50Tyr(p.D50Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_acceptor_variant |
| Transcription ID |
ENST00000262629 |
| Start |
35904635:35904635(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.277-1G>T |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TYROBP
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262629 |
| Start |
35907456:35907456(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.219G>C |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000262629 |
| Start |
35907537:35907537(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs760363848
|
| CDS Mutation |
c.138C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|