NM_000251.3(MSH2):c.2205C>A (p.Ile735=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Nov 14, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000579554.5
Allele description [Variation Report for NM_000251.3(MSH2):c.2205C>A (p.Ile735=)]
NM_000251.3(MSH2):c.2205C>A (p.Ile735=)
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
-
Tragopogon minor leafy/floricaula (LFY) gene, intron 2
Tragopogon minor leafy/floricaula (LFY) gene, intron 2gi|567498452|gb|KF050640.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024