Gene >> WNT5B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1645932:1645932(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs774388139
|
| CDS Mutation |
c.760G>A |
| AA Mutation |
p.Ala254Thr(p.A254T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1632840:1632840(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs200966877
|
| CDS Mutation |
c.263G>A |
| AA Mutation |
p.Arg88Gln(p.R88Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |