NM_000251.3(MSH2):c.2672T>G (p.Val891Gly) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000582667.7
Allele description [Variation Report for NM_000251.3(MSH2):c.2672T>G (p.Val891Gly)]
NM_000251.3(MSH2):c.2672T>G (p.Val891Gly)
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
-
Homo sapiens neuroligin 4 Y-linked (NLGN4Y), transcript variant 2, mRNA
Homo sapiens neuroligin 4 Y-linked (NLGN4Y), transcript variant 2, mRNAgi|256222831|ref|NM_001164238.1|Nucleotide
-
17q21.1 (14)
OMIM
-
MINPP1 [Mustela putorius furo]
MINPP1 [Mustela putorius furo]Gene ID:101692752Gene
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See more...Assertion and evidence details
Last Updated: May 1, 2024