Gene >> WNT5B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1645929:1645929(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.757G>C |
| AA Mutation |
p.Ala253Pro(p.A253P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000310594 |
| Start |
1632813:1632813(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.236G>A |
| AA Mutation |
p.Gly79Asp(p.G79D) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |