NM_007254.4(PNKP):c.678G>A (p.Lys226=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001531902.15
Allele description [Variation Report for NM_007254.4(PNKP):c.678G>A (p.Lys226=)]
NM_007254.4(PNKP):c.678G>A (p.Lys226=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024