NM_000251.3(MSH2):c.211G>C (p.Gly71Arg) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- May 15, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000985801.2
Allele description [Variation Report for NM_000251.3(MSH2):c.211G>C (p.Gly71Arg)]
NM_000251.3(MSH2):c.211G>C (p.Gly71Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
homo sapiens[Organism] AND IFNA16 AND (alive[prop]) (7)
Gene
-
homo sapiens[Organism] AND IFNA17 AND (alive[prop]) (11)
Gene
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Last Updated: Sep 29, 2024