G19S (p.Gly19Ser) variant of LAMA2 (Laminin subunit alpha-2)
G19S (p.Gly19Ser) in LAMA2 (Laminin subunit alpha-2) is a missense change. The record also includes variant effect predictions, population frequency data, and published literature.
G19S (p.Gly19Ser) variant details
- p.Gly19Ser
- gnomAD 6-128883300-G-A
- Missense
- REVEL 0.05
- CADD 17.50
- PolyPhen-2 0.00
- SIFT 0.41
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Literature evidence available