NM_017875.4(SLC25A38):c.*588T>A AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- May 16, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001672629.3
Allele description [Variation Report for NM_017875.4(SLC25A38):c.*588T>A]
NM_017875.4(SLC25A38):c.*588T>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024