NM_015102.5(NPHP4):c.4117C>T (p.Arg1373Trp) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002492092.1
Allele description [Variation Report for NM_015102.5(NPHP4):c.4117C>T (p.Arg1373Trp)]
NM_015102.5(NPHP4):c.4117C>T (p.Arg1373Trp)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023