NM_000179.3(MSH6):c.854G>T (p.Ser285Ile) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000556949.10
Allele description [Variation Report for NM_000179.3(MSH6):c.854G>T (p.Ser285Ile)]
NM_000179.3(MSH6):c.854G>T (p.Ser285Ile)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
calcium/calmodulin-dependent protein kinase kinase 1 isoform c [Homo sapiens]
calcium/calmodulin-dependent protein kinase kinase 1 isoform c [Homo sapiens]gi|1052292396|ref|NP_757343.2|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024