Colon Cancer: Gene >> LY6D
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301263 |
| Start |
142785313:142785313(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.295G>A |
| AA Mutation |
p.Ala99Thr(p.A99T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
splice_donor_variant |
| Transcription ID |
ENST00000301263 |
| Start |
142786464:142786464(version: GRCh38) |
| Mutation Type |
DEL |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.52+1delG |
| Mutation Classification |
Splice_Site |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LY6D
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000301263 |
| Start |
142785597:142785597(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769479466
|
| CDS Mutation |
c.143C>T |
| AA Mutation |
p.Thr48Met(p.T48M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|