| Mutation ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320122 |
| Start |
16551274:16551274(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs145877643
|
| CDS Mutation |
c.386C>T |
| AA Mutation |
p.Thr129Met(p.T129M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
4 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000320122 |
| Start |
16600746:16600746(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.115A>G |
| AA Mutation |
p.Lys39Glu(p.K39E) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> LMO3
| Mutation ID |
1 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000320122 |
| Start |
16551285:16551285(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.375C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|