NM_000179.3(MSH6):c.2149G>T (p.Val717Phe) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002424910.2
Allele description [Variation Report for NM_000179.3(MSH6):c.2149G>T (p.Val717Phe)]
NM_000179.3(MSH6):c.2149G>T (p.Val717Phe)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
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PREDICTED: Homo sapiens neuregulin 3 (NRG3), transcript variant X3, mRNA
PREDICTED: Homo sapiens neuregulin 3 (NRG3), transcript variant X3, mRNAgi|2462516619|ref|XM_054364609.1|Nucleotide
-
Athyma disjuncta voucher PM16_18 carbamoylphosphate synthase domain protein (CAD...
Athyma disjuncta voucher PM16_18 carbamoylphosphate synthase domain protein (CAD) gene, partial cdsgi|1953433219|gb|MW318306.1|Nucleotide
-
Arabidopsis thaliana pectin methylesterase 31 (PME31), mRNA
Arabidopsis thaliana pectin methylesterase 31 (PME31), mRNAgi|1063714482|ref|NM_113832.4|Nucleotide
-
Pseudomonas aeruginosa strain PAO1DF chromosome, complete genome
Pseudomonas aeruginosa strain PAO1DF chromosome, complete genomegi|2737409981|gb|CP157086.1|Nucleotide
-
Mutant Pseudomonas putida isolate FELIX_MS547, complete genome
Mutant Pseudomonas putida isolate FELIX_MS547, complete genomegi|2703320555|gb|CP148126.1|Nucleotide
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Last Updated: Sep 29, 2024