Variant ID | 23711 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |