Colon Cancer: Gene >> LMO2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395833 |
| Start |
33859360:33859360(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.473T>C |
| AA Mutation |
p.Ile158Thr(p.I158T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|
Rectum Cancer: Gene >> LMO2
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395833 |
| Start |
33859400:33859400(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs374739443
|
| CDS Mutation |
c.433G>A |
| AA Mutation |
p.Glu145Lys(p.E145K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000395833 |
| Start |
33859535:33859535(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.298C>T |
| AA Mutation |
p.Arg100Trp(p.R100W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
|