V142I (p.Val142Ile) variant of MCM3 (P25205)
V142I (p.Val142Ile) in MCM3 (P25205) 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 0.52 / 1. The record also includes population frequency data.
V142I (p.Val142Ile) variant details
- p.Val142Ile
- rs1033238760
- NCI-TCGA Cosmic COSV5771
- cosmic curated COSV57719
- gnomAD rs1033238760
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.517
- CADD 20.90
- PolyPhen-2 0.29
- SIFT 0.24
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)