C37G (p.Cys37Gly) variant of LAMC2 (Laminin subunit gamma-2)
C37G (p.Cys37Gly) in LAMC2 (Laminin subunit gamma-2) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.80 / 1. The record also includes population frequency data and structural context.
C37G (p.Cys37Gly) variant details
- p.Cys37Gly
- TOPMed rs1658945389
- gnomAD rs1658945389
- Missense
- Variant Prioritization Score for Impact Estimate 0.8
- REVEL 0.92
- CADD 26.40
- Most common in the HGDP:YAKUT population (allele frequency 0.04)
- Structural context available