NM_000251.3(MSH2):c.211+9C>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Oct 19, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000448740.12
Allele description [Variation Report for NM_000251.3(MSH2):c.211+9C>G]
NM_000251.3(MSH2):c.211+9C>G
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
-
DNA (cytosine-5)-methyltransferase 3B isoform X5 [Homo sapiens]
DNA (cytosine-5)-methyltransferase 3B isoform X5 [Homo sapiens]gi|2462579699|ref|XP_054179095.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024