H15N (p.His15Asn) variant of MCM6 (Q14566)
H15N (p.His15Asn) in MCM6 (Q14566) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
H15N (p.His15Asn) variant details
- p.His15Asn
- ExAC rs767901663
- gnomAD rs767901663
- Missense
- Variant Prioritization Score for Impact Estimate 0.296
- REVEL 0.06
- CADD 20.80
- PolyPhen-2 0.08
- SIFT 0.42
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available