R37G (p.Arg37Gly) variant of LAMA2 (Laminin subunit alpha-2)
R37G (p.Arg37Gly) in LAMA2 (Laminin subunit alpha-2) is a missense change. The record also includes variant effect predictions and population frequency data.
R37G (p.Arg37Gly) variant details
- p.Arg37Gly
- ExAC rs754399459
- Missense
- REVEL 0.13
- CADD 25.80
- PolyPhen-2 0.00
- SIFT 0.02
- Most common in the South Asian population (allele frequency 1.2e-05)