N69del (p.Asn69del) variant of DAP3 (P51398)
N69del (p.Asn69del) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.59 / 1. The record also includes population frequency data, published literature, and structural context.
N69del (p.Asn69del) variant details
- rs1658021470
- gnomAD 1-155721550-TACA-
- Inframe Deletion
- Variant Prioritization Score for Impact Estimate 0.588
- CADD 20.40
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available
- Literature evidence available