Overview

Variant ID 23711
Entrez Gene ID 51082
Gene POLR1D (GeneCards)
Location hg19 13:28270645-28270645
hg38 13:27696508-27696508
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000013.10:g.28270645 T>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 115169878

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.0275
CADD Raw score (version 1.3) -0.259924 (Deleterious)
FATHMM raw prediction score 0.40378 (Tolerated)
Deleterious probability by DeFine 0.0823 (Neutral)
Entrez Gene ID 51082 (NCBI Gene)
Official Gene Symbol POLR1D (GeneCards)
Number of variants in POLR1D in this database 3 (view all the variants)
Full name RNA polymerase I and III subunit D
Band 13q12.2
Other IDs Vega: OTTHUMG00000016635
OMIM: 613715
HGNC: HGNC:20422
Ensembl: ENSG00000186184
Other names AC19, RPA9, TCS2, RPA16, RPAC2, RPC16, POLR1C, RPO1-3
Summary The protein encoded by this gene is a component of the RNA polymerase I and RNA polymerase III complexes, which function in the synthesis of ribosomal RNA precursors and small RNAs, respectively. Mutations in this gene are a cause of Treacher Collins syndrome (TCS), a craniofacial development disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2011]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;