NM_000251.3(MSH2):c.34dup (p.Glu12fs) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Feb 14, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000221149.4
Allele description [Variation Report for NM_000251.3(MSH2):c.34dup (p.Glu12fs)]
NM_000251.3(MSH2):c.34dup (p.Glu12fs)
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
-
sperm microtubule inner protein 6 isoform 3 [Homo sapiens]
sperm microtubule inner protein 6 isoform 3 [Homo sapiens]gi|22219471|ref|NP_671698.1|Protein
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See more...Assertion and evidence details
Last Updated: Jun 9, 2024