NM_001099287.2(NIPAL4):c.544G>T (p.Val182Phe) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Nov 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003736742.2
Allele description [Variation Report for NM_001099287.2(NIPAL4):c.544G>T (p.Val182Phe)]
NM_001099287.2(NIPAL4):c.544G>T (p.Val182Phe)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024