A37A (p.Ala37Ala) variant of CLCN5 (P51795)
A37A (p.Ala37Ala) in CLCN5 (P51795) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data, published literature, and structural context.
A37A (p.Ala37Ala) variant details
- p.Ala37Ala
- rs1557187294
- gnomAD X-50042410-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.196
- CADD 8.38
- Most common in the Non-Finnish European population (allele frequency 2.5e-06)
- Structural context available
- Literature evidence available