P18S (p.Pro18Ser) variant of POLG (DNA polymerase subunit gamma-1)
P18S (p.Pro18Ser) in POLG (DNA polymerase subunit gamma-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Progressive sclerosing poliodystrophy. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
P18S (p.Pro18Ser) variant details
- p.Pro18Ser
- rs3087373
- ClinGen CA341889
- ClinVar RCV001851970
- UniProt VAR 014904
- Uncertain significance
- Progressive sclerosing poliodystrophy
- Missense
- Variant Prioritization Score for Impact Estimate 0.275
- REVEL 0.11
- CADD 17.60
- PolyPhen-2 0.00
- SIFT 0.29
- ClinVar: Uncertain significance (Progressive sclerosing poliodystrophy)
- EBI: Variant of uncertain significance (in dbSNP:rs3087373)
- UniProt: Uncertain significance (in dbSNP:rs3087373)
- Most common in the Latino/Admixed American population (allele frequency 2.8e-05)
- Structural context available
- Cited in: POLG-Related Disorders. (PMID 20301791)
- Cited in: Mitochondrial DNA Maintenance Defects Overview. (PMID 29517884)