Gene >> LGR5
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266674 |
| Start |
71584533:71584533(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.2523G>T |
| AA Mutation |
p.Trp841Cys(p.W841C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000266674 |
| Start |
71583887:71583887(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747564622
|
| CDS Mutation |
c.1877G>A |
| AA Mutation |
p.Arg626Gln(p.R626Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |