Overview

Variant ID 25868
Entrez Gene ID 348980
Gene HCN1 (GeneCards)
Location hg19 5:45315050-45315050
hg38 5:45314948-45314948
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000005.9:g.45315050 C>G (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 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3451
CADD Raw score (version 1.3) 0.14381 (Deleterious)
FATHMM raw prediction score 0.88943 (Tolerated)
Deleterious probability by DeFine 0.0397 (Neutral)
Entrez Gene ID 348980 (NCBI Gene)
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 #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID