NM_001191061.2(SLC25A22):c.636C>T (p.Asn212=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 10, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000983161.14
Allele description [Variation Report for NM_001191061.2(SLC25A22):c.636C>T (p.Asn212=)]
NM_001191061.2(SLC25A22):c.636C>T (p.Asn212=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024