Overview

Variant ID 24776
Entrez Gene ID 90134
Gene KCNH7 (GeneCards)
Location hg19 2:164296090-164296090
hg38 2:163439580-163439580
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000002.11:g.164296090 A>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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1483
CADD Raw score (version 1.3) -0.099218 (Deleterious)
FATHMM raw prediction score 0.10208 (Tolerated)
Deleterious probability by DeFine 0.4158 (Neutral)
Entrez Gene ID 90134 (NCBI Gene)
Official Gene Symbol KCNH7 (GeneCards)
Number of variants in KCNH7 in this database 5 (view all the variants)
Full name potassium voltage-gated channel subfamily H member 7
Band 2q24.2
Other IDs Vega: OTTHUMG00000132069
OMIM: 608169
HGNC: HGNC:18863
Ensembl: ENSG00000184611
Other names ERG3, HERG3, Kv11.3
Summary Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily H. This member is a pore-forming (alpha) subunit. There are at least two alternatively spliced transcript variants derived from this gene and encoding distinct isoforms. [provided by RefSeq, Jul 2008]

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