Overview

Variant ID 15727
Entrez Gene ID 55291
Gene PPP6R3 (GeneCards)
Location hg19 11:68375398-68375398
hg38 11:68607930-68607930
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000011.9:g.68375398 C>G (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 135006516

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.188
CADD Raw score (version 1.3) 0.60028 (Deleterious)
FATHMM raw prediction score 0.24875 (Tolerated)
Deleterious probability by DeFine 0.1391 (Neutral)
Entrez Gene ID 55291 (NCBI Gene)
Official Gene Symbol PPP6R3 (GeneCards)
Number of variants in PPP6R3 in this database 7 (view all the variants)
Full name protein phosphatase 6 regulatory subunit 3
Band 11q13.2
Other IDs Vega: OTTHUMG00000167596
OMIM: 610879
HGNC: HGNC:1173
Ensembl: ENSG00000110075
Other names SAPL, PP6R3, SAPLa, SAPS3, SAP190, C11orf23
Summary Protein phosphatase regulatory subunits, such as SAPS3, modulate the activity of protein phosphatase catalytic subunits by restricting substrate specificity, recruiting substrates, and determining the intracellular localization of the holoenzyme. SAPS3 is a regulatory subunit for the protein phosphatase-6 catalytic subunit (PPP6C; MIM 612725) (Stefansson and Brautigan, 2006 [PubMed 16769727]).[supplied by OMIM, Nov 2010]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;