Colon Cancer: Gene >> TXNDC12
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371626 |
| Start |
52055046:52055046(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.51C>A |
| AA Mutation |
p.Phe17Leu(p.F17L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000371626 |
| Start |
52024541:52024541(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200591679
|
| CDS Mutation |
c.324C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> TXNDC12
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000371626 |
| Start |
52024555:52024555(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.310G>T |
| AA Mutation |
p.Asp104Tyr(p.D104Y) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|