N38S (p.Asn38Ser) variant of DAP3 (P51398)
N38S (p.Asn38Ser) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
N38S (p.Asn38Ser) variant details
- p.Asn38Ser
- gnomAD 1-155717073-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.0978
- REVEL 0.05
- ESM-1b 0.00
- AlphaMissense 0.06
- CADD 7.45
- PolyPhen-2 0.00
- SIFT 0.82
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available