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Details for WNT10A:c.499G>C, p.Glu167Gln
| CHROMOSOME |
2 |
| GENOMIC COORDINATES |
| hg19 | hg38 |
|---|
| 219754828 | 218890106 |
|
| VARIANT EFFECT |
None |
| ANNOTATION FLAG |
None |
| GENE |
WNT10A |
| REFERENCE ALLELE |
G |
| ALTERNATE ALLELE |
C |
| TRANSCRIPT |
N.A. |
| CDNA CHANGE |
c.499G>C |
| PROTEIN CHANGE |
p.Glu167Gln |
| ALLELE FREQUENCY |
| 1KGP |
|---|
| Global | AFR | AMR | EAS | EUR | SAS |
|---|
| None | None | None | None | None | None |
| Gnomad |
|---|
| Global | AFR | AMR | ASJ | EAS | FIN | NFE | OTH | SAS |
|---|
| 1.99e-05 | 0.0 | 0.0 | 0.0 | 0.0002719 | 0.0 | 0.0 | 0.0 | 0.0 |
|
| PREDICTORS |
| sift | pp2 hvar | cadd | mutationtaster |
|---|
| Tolerated | Benign | 2.227015 | Disease causing |
|
| DBSNP ID |
NA |
| 1 combination linked to WNT10A:c.499G>C, p.Glu167Gln |
OLI938 |
| 1 disease linked to WNT10A:c.499G>C, p.Glu167Gln |
Hypodontia |
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