N15S (p.Asn15Ser) variant of ETV1 (ETS translocation variant 1)
N15S (p.Asn15Ser) in ETV1 (ETS translocation variant 1) 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 0.17 / 1. The record also includes population frequency data and structural context.
N15S (p.Asn15Ser) variant details
- p.Asn15Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.03
- CADD 20.80
- PolyPhen-2 0.00
- SIFT 0.77
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available