NM_020822.3(KCNT1):c.1317C>T (p.Asp439=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001506486.8
Allele description [Variation Report for NM_020822.3(KCNT1):c.1317C>T (p.Asp439=)]
NM_020822.3(KCNT1):c.1317C>T (p.Asp439=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024