A91V (p.Ala91Val) variant of XRCC3 (DNA repair protein XRCC3)
A91V (p.Ala91Val) in XRCC3 (DNA repair protein XRCC3) 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 0.07 / 1. The record also includes population frequency data and structural context.
A91V (p.Ala91Val) variant details
- p.Ala91Val
- rs1347713264
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10072
- TOPMed rs1347713264
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0743
- REVEL 0.03
- CADD 1.87
- PolyPhen-2 0.17
- SIFT 0.29
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Middle Eastern population (allele frequency 0.00019)
- Structural context available