NM_001366110.1(PAX4):c.868T>C (p.Cys290Arg) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002056864.6
Allele description [Variation Report for NM_001366110.1(PAX4):c.868T>C (p.Cys290Arg)]
NM_001366110.1(PAX4):c.868T>C (p.Cys290Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024