NM_000251.3(MSH2):c.2397T>C (p.Asn799=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000474873.9
Allele description [Variation Report for NM_000251.3(MSH2):c.2397T>C (p.Asn799=)]
NM_000251.3(MSH2):c.2397T>C (p.Asn799=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Dose Reconstruction for the Fernald Nuclear Facility
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intermittent explosive disorder
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C0021776[conceptid] (1)
MedGen
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Wdr72 WD repeat domain 72 [Mus musculus]
Wdr72 WD repeat domain 72 [Mus musculus]Gene ID:546144Gene
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GDS1760[ACCN] AND gsm[ETYP] (12)
GEO DataSets
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See more...Assertion and evidence details
Last Updated: May 7, 2024