rs1057520766
- Pathogenic
Your Genotype
Sign InDescription
The K511X nonsense variant in the EYA1 gene is predicted to cause loss of normalprotein function either through protein truncation or nonsense-mediated mRNA decay. The K511X variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Although this variant has not been reported previously to our knowledge, we consider it to be pathogenic.
Reference Allele
T
Alternative Allele
A
C
Chromosome
8
Location
71215453
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_000503.6(EYA1):c.1531A>T (p.Lys511Ter)
Allele
A
Clinical Significance
Pathogenic