NM_014425.5(INVS):c.625C>T (p.Pro209Ser) AND Nephronophthisis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001984869.2
Allele description [Variation Report for NM_014425.5(INVS):c.625C>T (p.Pro209Ser)]
NM_014425.5(INVS):c.625C>T (p.Pro209Ser)
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: Dec 24, 2023