Gene >> WNT6
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000233948 |
| Start |
218871133:218871133(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.187G>A |
| AA Mutation |
p.Ala63Thr(p.A63T) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000233948 |
| Start |
218873800:218873800(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs752458659
|
| CDS Mutation |
c.1053G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |