NM_001102416.3(KNG1):c.*1428C>T AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004153495.1
Allele description [Variation Report for NM_001102416.3(KNG1):c.*1428C>T]
NM_001102416.3(KNG1):c.*1428C>T
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 18, 2024