Variant ID | 8267 |
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Entrez Gene ID | 348980 |
Gene | HCN1 (GeneCards) |
Location | hg19 5:45678652-45678652
hg38 5:45678550-45678550 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.45678652 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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1086 |
CADD Raw score (version 1.3) | -0.119301 (Deleterious) |
FATHMM raw prediction score | 0.11926 (Tolerated) |
Deleterious probability by DeFine | 0.5721 (Deleterious) |
Entrez Gene ID | 348980 (NCBI Gene) |
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Official Gene Symbol | HCN1 (GeneCards) |
Number of variants in HCN1 in this database | 13 (view all the variants) |
Full name | hyperpolarization activated cyclic nucleotide gated potassium channel 1 |
Band | 5p12 |
Other IDs | Vega: OTTHUMG00000131155 OMIM: 602780 HGNC: HGNC:4845 Ensembl: ENSG00000164588 |
Other names | BCNG1, HAC-2, BCNG-1, EIEE24 |
Summary | The membrane protein encoded by this gene is a hyperpolarization-activated cation channel that contributes to the native pacemaker currents in heart and neurons. The encoded protein can homodimerize or heterodimerize with other pore-forming subunits to form a potassium channel. This channel may act as a receptor for sour tastes. [provided by RefSeq, Oct 2011] |
Individual ID | 29217584.13 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |