NM_000251.3(MSH2):c.1992C>G (p.Phe664Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000562025.4
Allele description [Variation Report for NM_000251.3(MSH2):c.1992C>G (p.Phe664Leu)]
NM_000251.3(MSH2):c.1992C>G (p.Phe664Leu)
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
-
Methodology - Stroke
Methodology - Stroke
-
NADH dehydrogenase subunit 4L (mitochondrion) [Rhabdias bufonis]
NADH dehydrogenase subunit 4L (mitochondrion) [Rhabdias bufonis]gi|2797671853|gb|XFH18075.1|Protein
-
cytochrome c oxidase subunit III (mitochondrion) [Rhabdias kafunata]
cytochrome c oxidase subunit III (mitochondrion) [Rhabdias kafunata]gi|2797671845|gb|XFH18068.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024