NM_004646.4(NPHS1):c.657G>A (p.Ala219=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001447121.6
Allele description [Variation Report for NM_004646.4(NPHS1):c.657G>A (p.Ala219=)]
NM_004646.4(NPHS1):c.657G>A (p.Ala219=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024