NM_014625.4(NPHS2):c.87C>G (p.Ala29=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 4, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000253074.8
Allele description [Variation Report for NM_014625.4(NPHS2):c.87C>G (p.Ala29=)]
NM_014625.4(NPHS2):c.87C>G (p.Ala29=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 4, 2024