NM_014801.4(PCNX2):c.3019G>A (p.Val1007Ile) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004095498.1
Allele description [Variation Report for NM_014801.4(PCNX2):c.3019G>A (p.Val1007Ile)]
NM_014801.4(PCNX2):c.3019G>A (p.Val1007Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 9, 2024