N41D (p.Asn41Asp) variant of ADA (Adenosine deaminase)
N41D (p.Asn41Asp) in ADA (Adenosine deaminase) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
N41D (p.Asn41Asp) variant details
- p.Asn41Asp
- gnomAD rs2065409692
- Missense
- Variant Prioritization Score for Impact Estimate 0.202
- REVEL 0.29
- CADD 0.17
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available