R37I (p.Arg37Ile) variant of LAMA2 (Laminin subunit alpha-2)
R37I (p.Arg37Ile) 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.
R37I (p.Arg37Ile) variant details
- p.Arg37Ile
- NCI-TCGA Cosmic COSV7034
- cosmic curated COSV70342
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.13
- CADD 33.00
- PolyPhen-2 0.45
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the East Asian population (allele frequency 2.6e-05)