Gene >> WNT7A
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000285018 |
| Start |
13819282:13819282(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.712G>A |
| AA Mutation |
p.Val238Met(p.V238M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000285018 |
| Start |
13819289:13819289(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs536761427
|
| CDS Mutation |
c.705C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |