R29W (p.Arg29Trp) variant of LAMA2 (Laminin subunit alpha-2)
R29W (p.Arg29Trp) in LAMA2 (Laminin subunit alpha-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and population frequency data.
R29W (p.Arg29Trp) variant details
- p.Arg29Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.07
- CADD 21.90
- PolyPhen-2 0.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the South Asian population (allele frequency 1.2e-05)