I13N (p.Ile13Asn) variant of DAP3 (P51398)
I13N (p.Ile13Asn) in DAP3 (P51398) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
I13N (p.Ile13Asn) variant details
- p.Ile13Asn
- TOPMed rs1470221997
- gnomAD rs1470221997
- Missense
- Variant Prioritization Score for Impact Estimate 0.135
- REVEL 0.10
- ESM-1b 0.00
- AlphaMissense 0.06
- CADD 13.80
- PolyPhen-2 0.00
- SIFT 0.21
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available