Gene >> LATS1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253339 |
| Start |
149661865:149661865(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.3257A>T |
| AA Mutation |
p.Asp1086Val(p.D1086V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000253339 |
| Start |
149702045:149702045(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs191160444
|
| CDS Mutation |
c.82C>T |
| AA Mutation |
p.Arg28Trp(p.R28W) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |