NM_001278689.2(EOGT):c.1467G>A (p.Pro489=) AND Adams-Oliver syndrome 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003070397.3
Allele description [Variation Report for NM_001278689.2(EOGT):c.1467G>A (p.Pro489=)]
NM_001278689.2(EOGT):c.1467G>A (p.Pro489=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024