NM_000891.3(KCNJ2):c.155G>T (p.Gly52Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000627123.2
Allele description [Variation Report for NM_000891.3(KCNJ2):c.155G>T (p.Gly52Val)]
NM_000891.3(KCNJ2):c.155G>T (p.Gly52Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
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Homologene neighbors for GEO Profiles (Select 132101847) (0)
GEO Profiles
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Homo sapiens chromosome 18, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 18, GRCh38.p14 Primary Assemblygi|568815580|gnl|ASM:GCF_000001305| f|NC_000018.10||gpp|GPC_000001310.1||gnl|NCBI_GENOMES|18Nucleotide
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Profile neighbors for GEO Profiles (Select 132536804) (68)
GEO Profiles
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Chromosome neighbors for GEO Profiles (Select 132548793) (20)
GEO Profiles
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Chromosome neighbors for GEO Profiles (Select 71237180) (20)
GEO Profiles
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Last Updated: Jun 24, 2023