NM_005660.3(SLC35A2):c.1077C>T (p.Cys359=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002420925.2
Allele description [Variation Report for NM_005660.3(SLC35A2):c.1077C>T (p.Cys359=)]
NM_005660.3(SLC35A2):c.1077C>T (p.Cys359=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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PopSet Links for Nucleotide (Select 1436199067) (1)
PopSet
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Homologene neighbors for GEO Profiles (Select 50692919) (0)
GEO Profiles
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Homo sapiens chromosome 4, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 4, GRCh38.p14 Primary Assemblygi|568815594|gnl|ASM:GCF_000001305| |NC_000004.12||gpp|GPC_000001296.1||gnl|NCBI_GENOMES|4Nucleotide
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Taxonomy Links for Nucleotide (Select 1436199051) (1)
Taxonomy
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Taxonomy Links for Protein (Select 82083438) (1)
Taxonomy
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Last Updated: Sep 29, 2024