NM_153240.5(NPHP3):c.3816T>C (p.Tyr1272=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002495591.1
Allele description [Variation Report for NM_153240.5(NPHP3):c.3816T>C (p.Tyr1272=)]
NM_153240.5(NPHP3):c.3816T>C (p.Tyr1272=)
Condition(s)
Assertion and evidence details
Last Updated: Jul 15, 2024