NM_000251.3(MSH2):c.266T>C (p.Val89Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Nov 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000215101.13
Allele description [Variation Report for NM_000251.3(MSH2):c.266T>C (p.Val89Ala)]
NM_000251.3(MSH2):c.266T>C (p.Val89Ala)
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
-
Transcriptional factor B3 family protein [Arabidopsis thaliana]
Transcriptional factor B3 family protein [Arabidopsis thaliana]gi|30689117|ref|NP_194896.2|Protein
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GPRIN3 AND (alive[prop]) (562)
Gene
-
L1TD1 AND (alive[prop]) (186)
Gene
-
Gm29788 predicted gene, 29788 [Mus musculus]
Gm29788 predicted gene, 29788 [Mus musculus]Gene ID:101056148Gene
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024