NM_000251.3(MSH2):c.119G>T (p.Gly40Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000221582.3
Allele description [Variation Report for NM_000251.3(MSH2):c.119G>T (p.Gly40Val)]
NM_000251.3(MSH2):c.119G>T (p.Gly40Val)
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
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Ophiomyxa vivipara isolate OvivSAO22 cytochrome c oxidase subunit I (COI) gene, ...
Ophiomyxa vivipara isolate OvivSAO22 cytochrome c oxidase subunit I (COI) gene, partial cds; mitochondrialgi|566073135|gb|KF663503.1|Nucleotide
-
cytochrome oxidase subunit 1, partial (mitochondrion) [Priacanthus blochii]
cytochrome oxidase subunit 1, partial (mitochondrion) [Priacanthus blochii]gi|2722342103|gb|WZX07064.1|Protein
-
cytochrome c oxidase subunit I, partial (mitochondrion) [Priacanthus blochii]
cytochrome c oxidase subunit I, partial (mitochondrion) [Priacanthus blochii]gi|2515602960|gb|WIM34567.1|Protein
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Last Updated: Sep 29, 2024