S45G (p.Ser45Gly) variant of LAG3 (P18627)
S45G (p.Ser45Gly) in LAG3 (P18627) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
S45G (p.Ser45Gly) variant details
- p.Ser45Gly
- rs533786810
- ClinGen CA6415182
- cosmic curated COSV10506
- ClinVar RCV004407167
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.149
- REVEL 0.02
- CADD 23.10
- PolyPhen-2 0.00
- SIFT 0.01
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the 1KG:BEB population (allele frequency 0.0051)
- Structural context available