NM_000179.3(MSH6):c.4001+19T>C AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002189655.6
Allele description [Variation Report for NM_000179.3(MSH6):c.4001+19T>C]
NM_000179.3(MSH6):c.4001+19T>C
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
sphingomyelin phosphodiesterase 4 isoform 2 [Homo sapiens]
sphingomyelin phosphodiesterase 4 isoform 2 [Homo sapiens]gi|102467481|ref|NP_060421.2|Protein
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Physiology, Pulse Pressure - StatPearls
Physiology, Pulse Pressure - StatPearls
-
Flecainide - Drugs and Lactation Database (LactMed®)
Flecainide - Drugs and Lactation Database (LactMed®)
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024