S6C (p.Ser6Cys) variant of HNRNPA1 (P09651)
S6C (p.Ser6Cys) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
S6C (p.Ser6Cys) variant details
- p.Ser6Cys
- TOPMed rs1944167400
- gnomAD rs1944167400
- Missense
- Variant Prioritization Score for Impact Estimate 0.556
- REVEL 0.41
- CADD 25.80
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available