S37G (p.Ser37Gly) variant of ITGB4 (Integrin beta-4)
S37G (p.Ser37Gly) in ITGB4 (Integrin beta-4) 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 0.65 / 1. The record also includes population frequency data and structural context.
S37G (p.Ser37Gly) variant details
- p.Ser37Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.654
- REVEL 0.81
- CADD 26.90
- PolyPhen-2 0.56
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available