NM_000218.3(KCNQ1):c.858C>T (p.Asp286=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 24, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001700200.11
Allele description [Variation Report for NM_000218.3(KCNQ1):c.858C>T (p.Asp286=)]
NM_000218.3(KCNQ1):c.858C>T (p.Asp286=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 13, 2024