NM_000251.3(MSH2):c.463G>A (p.Val155Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002334780.2
Allele description [Variation Report for NM_000251.3(MSH2):c.463G>A (p.Val155Ile)]
NM_000251.3(MSH2):c.463G>A (p.Val155Ile)
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
-
W8CLH7 (0)
Protein
-
hypothetical protein BIW12_06660 [Flavobacterium commune]
hypothetical protein BIW12_06660 [Flavobacterium commune]gi|1095442028|gnl|PRJNA343870|BIW12 0|gb|AOZ99145.1|Protein
-
S41 family peptidase [Prevotella scopos JCM 17725]
S41 family peptidase [Prevotella scopos JCM 17725]gi|2028838254|gnl|PRJNA282954|J4856 0|gb|QUB45732.1|Protein
-
Macaca mulatta CD94 mRNA, complete cds
Macaca mulatta CD94 mRNA, complete cdsgi|11344843|gb|AF294886.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024