NM_004646.4(NPHS1):c.1396T>C (p.Leu466=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001450491.6
Allele description [Variation Report for NM_004646.4(NPHS1):c.1396T>C (p.Leu466=)]
NM_004646.4(NPHS1):c.1396T>C (p.Leu466=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024