NM_000251.3(MSH2):c.2358del (p.Glu786fs) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Sep 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002448495.2
Allele description [Variation Report for NM_000251.3(MSH2):c.2358del (p.Glu786fs)]
NM_000251.3(MSH2):c.2358del (p.Glu786fs)
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
-
PREDICTED: Vicugna pacos inositol polyphosphate-4-phosphatase type II B (INPP4B)...
PREDICTED: Vicugna pacos inositol polyphosphate-4-phosphatase type II B (INPP4B), transcript variant X2, mRNAgi|1777462781|ref|XM_015249488.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024