NM_172201.2(KCNE2):c.261C>T (p.Tyr87=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000126407.5
Allele description [Variation Report for NM_172201.2(KCNE2):c.261C>T (p.Tyr87=)]
NM_172201.2(KCNE2):c.261C>T (p.Tyr87=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 1, 2024