S41N (p.Ser41Asn) variant of FOXP2 (Forkhead box protein P2)
S41N (p.Ser41Asn) in FOXP2 (Forkhead box protein P2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
S41N (p.Ser41Asn) variant details
- p.Ser41Asn
- NCI-TCGA Cosmic COSV6348
- cosmic curated COSV63482
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.4
- REVEL 0.15
- CADD 22.30
- PolyPhen-2 0.29
- SIFT 1.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available