V66M (p.Val66Met) variant of MCM6 (Q14566)
V66M (p.Val66Met) in MCM6 (Q14566) 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 0.13 / 1. The record also includes population frequency data and structural context.
V66M (p.Val66Met) variant details
- p.Val66Met
- rs1558764542
- NCI-TCGA Cosmic COSV5146
- Ensembl rs1558764542
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.128
- REVEL 0.02
- CADD 15.00
- PolyPhen-2 0.02
- SIFT 0.13
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available