NM_000890.5(KCNJ5):c.744G>A (p.Glu248=) AND Congenital long QT syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000260142.5
Allele description [Variation Report for NM_000890.5(KCNJ5):c.744G>A (p.Glu248=)]
NM_000890.5(KCNJ5):c.744G>A (p.Glu248=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024