A33T (p.Ala33Thr) variant of LAMA2 (Laminin subunit alpha-2)
A33T (p.Ala33Thr) 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.
A33T (p.Ala33Thr) variant details
- p.Ala33Thr
- rs1362087620
- NCI-TCGA Cosmic COSV1013
- cosmic curated COSV10137
- TOPMed rs1362087620
- Variant assessed as somatic; moderate impact.
- Missense
- REVEL 0.11
- CADD 20.40
- PolyPhen-2 0.00
- SIFT 0.30
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)