NM_001126121.2(SLC25A19):c.484G>A (p.Val162Met) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002150412.5
Allele description [Variation Report for NM_001126121.2(SLC25A19):c.484G>A (p.Val162Met)]
NM_001126121.2(SLC25A19):c.484G>A (p.Val162Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024