N41H (p.Asn41His) variant of CTNNA1 (Catenin alpha-1)
N41H (p.Asn41His) in CTNNA1 (Catenin alpha-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes structural context.
N41H (p.Asn41His) variant details
- p.Asn41His
- rs1755321895
- ClinGen CA361477287
- ClinVar RCV001238688
- Ensembl rs1755321895
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.407
- AlphaMissense 0.40
- MetaLR 0.25
- MetaSVM -0.59
- PolyPhen-2 0.01
- SIFT 0.00
- EVE 0.44
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available