NM_000891.3(KCNJ2):c.773T>C (p.Ile258Thr) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 16, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000126416.3
Allele description [Variation Report for NM_000891.3(KCNJ2):c.773T>C (p.Ile258Thr)]
NM_000891.3(KCNJ2):c.773T>C (p.Ile258Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022