NM_014625.4(NPHS2):c.246G>T (p.Ala82=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003701402.2
Allele description [Variation Report for NM_014625.4(NPHS2):c.246G>T (p.Ala82=)]
NM_014625.4(NPHS2):c.246G>T (p.Ala82=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024