P37A (p.Pro37Ala) variant of ATP6V1B1 (P15313)
P37A (p.Pro37Ala) in ATP6V1B1 (P15313) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Renal tubular acidosis with progressive nerve deafness. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data and structural context.
P37A (p.Pro37Ala) variant details
- p.Pro37Ala
- ExAC rs782369259
- TOPMed rs782369259
- gnomAD rs782369259
- Uncertain significance
- Renal tubular acidosis with progressive nerve deafness
- Missense
- Variant Prioritization Score for Impact Estimate 0.599
- REVEL 0.50
- CADD 22.80
- PolyPhen-2 0.24
- SIFT 0.01
- ClinVar: Uncertain significance (Renal tubular acidosis with progressive nerve deafness)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available