Overview

Variant ID 6342
Entrez Gene ID 5431
Gene POLR2B (GeneCards)
Location hg19 4:57888394-57888394
hg38 4:57022228-57022228
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.57888394 A>C (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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.0898
CADD Raw score (version 1.3) 3.315591 (Deleterious)
FATHMM raw prediction score 0.95272 (Tolerated)
SIFT score 0.056 (Tolerated)
LRT score 0 (Tolerated)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 1.465 (Tolerated)
PROVEAN score -2.84 (Deleterious)
MetaSVM score -0.737 (Tolerated)
MetaLR score 0.216 (Tolerated)
MCAP score 0.036 (Deleterious)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 4.56
PhyloP score based on multiple alignment of 100 vertebrates 6.044
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 12.896
Deleterious probability by iFish2 0.9151 (Deleterious)
Deleterious probability by DeFine 0.9568 (Deleterious)
Entrez Gene ID 5431 (NCBI Gene)
Official Gene Symbol POLR2B (GeneCards)
Number of variants in POLR2B in this database 2 (view all the variants)
Full name RNA polymerase II subunit B
Band 4q12
Other IDs Vega: OTTHUMG00000128771
OMIM: 180661
HGNC: HGNC:9188
Ensembl: ENSG00000047315
Other names RPB2, POL2RB, hRPB140
Summary This gene encodes the second largest subunit of RNA polymerase II (Pol II), a DNA-dependent RNA polymerase that catalyzes the transcription of DNA into precursors of mRNA, snRNA and microRNA. This subunit and the largest subunit form opposite sides of the center cleft of Pol II. Deletion of the flap loop region of this subunit results in a decrease in the rate of transcriptional elongation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

Individual #1

Individual ID 29217584.08 (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;