NM_000251.3(MSH2):c.1857T>C (p.Tyr619=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001806169.4
Allele description [Variation Report for NM_000251.3(MSH2):c.1857T>C (p.Tyr619=)]
NM_000251.3(MSH2):c.1857T>C (p.Tyr619=)
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
-
Cenococcum geophilum 18S ribosomal RNA gene, partial sequence; internal transcri...
Cenococcum geophilum 18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence.PopSet: 530341882PopSet
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024