V91A (p.Val91Ala) variant of TGM1 (P22735)
V91A (p.Val91Ala) in TGM1 (P22735) 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 0.16 / 1. The record also includes population frequency data and structural context.
V91A (p.Val91Ala) variant details
- p.Val91Ala
- rs1484506489
- TOPMed rs1484506489
- gnomAD rs1484506489
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.162
- REVEL 0.18
- CADD 0.09
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available