Gene >> SMO
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249373 |
| Start |
129205664:129205664(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.802T>C |
| AA Mutation |
p.Phe268Leu(p.F268L) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000249373 |
| Start |
129205271:129205271(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.606C>A |
| AA Mutation |
p.Asn202Lys(p.N202K) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |