S4T (p.Ser4Thr) variant of HNRNPA1 (P09651)
S4T (p.Ser4Thr) in HNRNPA1 (P09651) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data, published literature, and structural context.
S4T (p.Ser4Thr) variant details
- p.Ser4Thr
- rs1257601954
- gnomAD 12-54281032-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.469
- CADD 8.33
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available
- Literature evidence available