NM_000251.3(MSH2):c.77T>C (p.Met26Thr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001026826.3
Allele description [Variation Report for NM_000251.3(MSH2):c.77T>C (p.Met26Thr)]
NM_000251.3(MSH2):c.77T>C (p.Met26Thr)
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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Aspergillus terreus NIH2624 uncharacterized protein (ATEG_01425), partial mRNA
Aspergillus terreus NIH2624 uncharacterized protein (ATEG_01425), partial mRNAgi|115384485|ref|XM_001208790.1|Nucleotide
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Kcnk3 AND (alive[prop]) (505)
Gene
-
Homologene neighbors for GEO Profiles (Select 46500595) (0)
GEO Profiles
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Chromosome neighbors for GEO Profiles (Select 74268339) (20)
GEO Profiles
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TCF7L2 transcription factor 7 like 2 [Homo sapiens]
TCF7L2 transcription factor 7 like 2 [Homo sapiens]Gene ID:6934Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024