NM_172107.4(KCNQ2):c.2052C>T (p.Gly684=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 15, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000358268.4
Allele description [Variation Report for NM_172107.4(KCNQ2):c.2052C>T (p.Gly684=)]
NM_172107.4(KCNQ2):c.2052C>T (p.Gly684=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024