NM_001023570.4(IQCB1):c.1656C>G (p.Ala552=) AND Nephronophthisis
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 23, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002070777.6
Allele description [Variation Report for NM_001023570.4(IQCB1):c.1656C>G (p.Ala552=)]
NM_001023570.4(IQCB1):c.1656C>G (p.Ala552=)
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: Sep 29, 2024