NM_000179.3(MSH6):c.1991C>G (p.Ser664Ter) AND not provided
- Germline classification:
- Pathogenic (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001795759.2
Allele description [Variation Report for NM_000179.3(MSH6):c.1991C>G (p.Ser664Ter)]
NM_000179.3(MSH6):c.1991C>G (p.Ser664Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Hgsnat heparan-alpha-glucosaminide N-acetyltransferase [Rattus norvegicus]
Hgsnat heparan-alpha-glucosaminide N-acetyltransferase [Rattus norvegicus]Gene ID:361165Gene
-
Homo sapiens chromosome 7, GRCh38.p14 Primary Assembly
Homo sapiens chromosome 7, GRCh38.p14 Primary Assemblygi|568815591|gnl|ASM:GCF_000001305| |NC_000007.14||gpp|GPC_000001299.1||gnl|NCBI_GENOMES|7Nucleotide
-
Full text in PMC (nucleotide) for Gene (Select 102548228) (1)
PMC
-
nucleolar protein 9 isoform X1 [Homo sapiens]
nucleolar protein 9 isoform X1 [Homo sapiens]gi|2462539110|ref|XP_054231488.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024