NM_001382422.1(EXOC3L2):c.1685G>A (p.Arg562His) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002972505.2
Allele description [Variation Report for NM_001382422.1(EXOC3L2):c.1685G>A (p.Arg562His)]
NM_001382422.1(EXOC3L2):c.1685G>A (p.Arg562His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 2, 2024