NM_020822.3(KCNT1):c.3162C>T (p.His1054=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 16, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000420648.10
Allele description [Variation Report for NM_020822.3(KCNT1):c.3162C>T (p.His1054=)]
NM_020822.3(KCNT1):c.3162C>T (p.His1054=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 16, 2024