Gene >> WNT9A
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272164 |
| Start |
227921615:227921615(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1001T>C |
| AA Mutation |
p.Val334Ala(p.V334A) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000272164 |
| Start |
227924187:227924187(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.566A>G |
| AA Mutation |
p.Lys189Arg(p.K189R) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |