Gene >> WNT8B
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343737 |
| Start |
100482676:100482676(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs769222868
|
| CDS Mutation |
c.916G>A |
| AA Mutation |
p.Val306Met(p.V306M) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000343737 |
| Start |
100479956:100479956(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs747723999
|
| CDS Mutation |
c.185G>A |
| AA Mutation |
p.Arg62His(p.R62H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |