NM_000162.5(GCK):c.501G>T (p.Trp167Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 21, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001765792.2
Allele description [Variation Report for NM_000162.5(GCK):c.501G>T (p.Trp167Cys)]
NM_000162.5(GCK):c.501G>T (p.Trp167Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC101930171 [Homo sapiens]
LOC101930171 [Homo sapiens]Gene ID:101930171Gene
-
Hemoglobin C Disease
Hemoglobin C DiseaseA disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and...<br/>Year introduced: 1972(1966)MeSH
-
"73-66-5"[CompleteSynonym] (1)
PubChem Compound
-
cytochrome c oxidase assembly protein COX19-like isoform X2 [Cucurbita moschata]
cytochrome c oxidase assembly protein COX19-like isoform X2 [Cucurbita moschata]gi|1279820896|ref|XP_022964209.1|Protein
-
pentatricopeptide repeat-containing protein At4g30825, chloroplastic [Cucumis sa...
pentatricopeptide repeat-containing protein At4g30825, chloroplastic [Cucumis sativus]gi|449457967|ref|XP_004146719.1|Protein
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023