Overview

Variant ID 32340
Entrez Gene ID 23236
Gene PLCB1 (GeneCards)
Location hg19 20:8130965-8130965
hg38 20:8150318-8150318
Disease Asymptomatic
Method NGS gene panel
Mutation(HGVS format) NC_000020.10:g.8130965 A>T (Genome Assembly: hg19)

Other information

Exon or Intron Exon
Position in protein 42
Amino acid changes in protein I > F
Position in cDNA 124
Changes in cDNA A > T
mRNA accession NA
mRNA length NA
Reference length 63025520

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0077
CADD Raw score (version 1.3) 4.160062 (Deleterious)
FATHMM raw prediction score 0.93778 (Tolerated)
SIFT score 0.035 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 0.993 (Deleterious)
MutatioinAssessor score 0.805 (Tolerated)
PROVEAN score -1.44 (Tolerated)
MetaSVM score -0.989 (Tolerated)
MetaLR score 0.142 (Tolerated)
MCAP score 0.012 (Tolerated)
FitCons score 0.539 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.76
PhyloP score based on multiple alignment of 100 vertebrates 4.056
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 14.891
Deleterious probability by iFish2 0.4521 (Neutral)
Deleterious probability by DeFine 0.959 (Deleterious)
Entrez Gene ID 23236 (NCBI Gene)
Official Gene Symbol PLCB1 (GeneCards)
Number of variants in PLCB1 in this database 66 (view all the variants)
Full name phospholipase C beta 1
Band 20p12.3
Other IDs Vega: OTTHUMG00000031849
OMIM: 607120
HGNC: HGNC:15917
Ensembl: ENSG00000182621
Other names PLC-I, EIEE12, PI-PLC, PLC154, PLCB1A, PLCB1B, PLC-154, PLC-beta-1
Summary The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of many extracellular signals. This gene is activated by two G-protein alpha subunits, alpha-q and alpha-11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 25999502.02 (view all the variants in this individual)
Pubmed ID 25999502
Whose mosaic mutation Normal  
Origin of mosaic mutation in patients de novo
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 25999502

Pubmed ID 25999502
Title High burden and pervasive positive selection of somatic mutations in normal human skin
Journal Science
Publication date 2015.05
Disease Asymptomatic
Number of cases Male cases: 1; Female cases: 3;