ClinVar Miner

Submissions for variant NM_020632.3(ATP6V0A4):c.2308C>T (p.Arg770Ter) (rs754517968)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000779530 SCV000916192 likely pathogenic Renal tubular acidosis, distal, autosomal recessive 2017-07-11 criteria provided, single submitter clinical testing The ATP6V0A4 c.2308C>T (p.Arg770Ter) variant is a stop-gained variant that is predicted to result in premature termination of the protein. This variant has been reported in two studies in which it is found in a total of five individuals with autosomal recessive distal renal tubular acidosis, including in three, of which two were related, who carried the variant in a homozygous state, and in two siblings who carried the variant in a compound heterozygote state (Vargas-Poussou et al. 2006; Swayamprakasam et al. 2010). Vargas-Poussou et al. (2006) identified the three homozygotes in two separate Malian families with identical haplotypes, suggesting a possible founder effect. In the first family, the proband was affected with both nephrocalcinosis and sensorineural hearing loss while the proband from the second family had neither nephrocalcinosis or sensorineural hearing loss. The affected mother and an affected uncle in the second family both had nephrocalcinosis and sensorineural hearing loss, however no genotype information was given for the affected uncle. The compound heterozygous siblings reported in Swayamprakasam et al. (2010) were affected with both distal renal tubular acidosis and bilateral sensorineural hearing loss and carried a missense variant on the second allele that was confirmed by parental sequencing. Control data are unavailable for the p.Arg770Ter variant, which is reported at a frequency of 0.000916 in the Ashkenazi Jewish population in the Genome Aggregation Database. Based on the evidence from the literature and due to the potential impact of stop-gained variants, the p.Arg770Ter variant is classified as likely pathogenic for autosomal recessive distal renal tubular acidosis. This variant was observed by ICSL as part of a predisposition screen in an ostensibly healthy population.

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