Variant ID | 33607 |
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Entrez Gene ID | 23236 |
Gene | PLCB1 (GeneCards) |
Location | hg19 20:8709728-8709728
hg38 20:8729081-8729081 |
Disease | Asymptomatic |
Method | NGS gene panel |
Mutation(HGVS format) | NC_000020.10:g.8709728 C>T (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 599 |
Amino acid changes in protein | P > S |
Position in cDNA | 1795 |
Changes in cDNA | C > T |
mRNA accession | NA |
mRNA length | NA |
Reference length | 63025520 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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Variant IDs in COSMIC (version 89) | 1713169 |
Variant occurences in COSMIC | 1(skin) |
EIGEN score | 1.11 |
CADD Raw score (version 1.3) | 6.654253 (Deleterious) |
FATHMM raw prediction score | 0.98087 (Tolerated) |
SIFT score | 0 (Deleterious) |
LRT score | 0 (Deleterious) |
MutationTaster score | 1 (Deleterious) |
MutatioinAssessor score | 4.19 (Deleterious) |
PROVEAN score | -7.07 (Deleterious) |
MetaSVM score | 0.901 (Deleterious) |
MetaLR score | 0.822 (Deleterious) |
MCAP score | 0.444 (Deleterious) |
FitCons score | 0.638 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 5.83 |
PhyloP score based on multiple alignment of 100 vertebrates | 7.905 |
PhastCons score based on multiple alignment of 100 vertebrates | 1 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 20.121 |
Deleterious probability by iFish2 | 0.9966 (Deleterious) |
Deleterious probability by DeFine | 0.8796 (Deleterious) |
Entrez Gene ID | 23236 (NCBI Gene) |
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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 ID | 25999502.03 (view all the variants in this individual) |
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Pubmed ID | 25999502 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 25999502 |
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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; |