H51N (p.His51Asn) variant of ITGA6 (Integrin alpha-6)
H51N (p.His51Asn) in ITGA6 (Integrin alpha-6) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data and structural context.
H51N (p.His51Asn) variant details
- p.His51Asn
- gnomAD rs1372698008
- Missense
- Variant Prioritization Score for Impact Estimate 0.753
- CADD 26.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available