NM_004646.4(NPHS1):c.1113G>A (p.Leu371=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003692625.2
Allele description [Variation Report for NM_004646.4(NPHS1):c.1113G>A (p.Leu371=)]
NM_004646.4(NPHS1):c.1113G>A (p.Leu371=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024