NM_014625.4(NPHS2):c.954C>T (p.Ala318=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Jul 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243457.9
Allele description [Variation Report for NM_014625.4(NPHS2):c.954C>T (p.Ala318=)]
NM_014625.4(NPHS2):c.954C>T (p.Ala318=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024