G44S (p.Gly44Ser) variant of SLC22A2 (O15244)
G44S (p.Gly44Ser) in SLC22A2 (O15244) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data and structural context.
G44S (p.Gly44Ser) variant details
- p.Gly44Ser
- NCI-TCGA Cosmic COSV6526
- cosmic curated COSV65266
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.638
- REVEL 0.53
- CADD 26.50
- PolyPhen-2 0.96
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available