Variant ID | 30965 |
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Entrez Gene ID | 27133 |
Gene | KCNH5 (GeneCards) |
Location | hg19 14:63174328-63174328
hg38 14:62707610-62707610 |
Disease | Asymptomatic |
Method | NGS gene panel |
Mutation(HGVS format) | NC_000014.8:g.63174328 G>A (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 955 |
Amino acid changes in protein | S > S |
Position in cDNA | 2865 |
Changes in cDNA | C > T |
mRNA accession | NA |
mRNA length | NA |
Reference length | 107349540 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 1.2616 |
CADD Raw score (version 1.3) | -0.305017 (Deleterious) |
FATHMM raw prediction score | 0.97927 (Tolerated) |
Deleterious probability by DeFine | 0.8209 (Deleterious) |
Entrez Gene ID | 27133 (NCBI Gene) |
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Official Gene Symbol | KCNH5 (GeneCards) |
Number of variants in KCNH5 in this database | 35 (view all the variants) |
Full name | potassium voltage-gated channel subfamily H member 5 |
Band | 14q23.2 |
Other IDs | Vega: OTTHUMG00000029041 OMIM: 605716 HGNC: HGNC:6254 Ensembl: ENSG00000140015 |
Other names | EAG2, hEAG2, H-EAG2, Kv10.2 |
Summary | This gene encodes a member of voltage-gated potassium channels. Members of this family have diverse functions, including regulating neurotransmitter and hormone release, cardiac function, and cell volume. This protein is an outward-rectifying, noninactivating channel. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
Individual ID | 25999502.01 (view all the variants in this individual) |
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Pubmed ID | 25999502 |
Whose mosaic mutation | Normal |
Origin of mosaic mutation in patients | de novo |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 25999502 |
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Title | High burden and pervasive positive selection of somatic mutations in normal human skin |
Journal | Science |
Publication date | 2015.05 |
Disease | Asymptomatic |
Number of cases | Male cases: 1; Female cases: 3; |