NM_015102.5(NPHP4):c.4093C>T (p.His1365Tyr) AND Nephronophthisis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002050326.5
Allele description [Variation Report for NM_015102.5(NPHP4):c.4093C>T (p.His1365Tyr)]
NM_015102.5(NPHP4):c.4093C>T (p.His1365Tyr)
Condition(s)
- Name:
- Nephronophthisis
- Synonyms:
- juvenile nephronophthisis
- Identifiers:
- MONDO: MONDO:0019005; MedGen: C0687120; OMIM: PS256100; Human Phenotype Ontology: HP:0000090
Assertion and evidence details
Last Updated: Feb 28, 2024