S13N (p.Ser13Asn) variant of KRT3 (Keratin, type II cytoskeletal 3)
S13N (p.Ser13Asn) in KRT3 (Keratin, type II cytoskeletal 3) 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.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- TOPMed rs1182160925
- gnomAD rs1182160925
- Missense
- Variant Prioritization Score for Impact Estimate 0.2
- REVEL 0.17
- CADD 10.30
- Most common in the HGDP:FRENCH population (allele frequency 0.019)
- Structural context available