NM_017547.4(FOXRED1):c.576G>A (p.Gln192=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003560477.1
Allele description [Variation Report for NM_017547.4(FOXRED1):c.576G>A (p.Gln192=)]
NM_017547.4(FOXRED1):c.576G>A (p.Gln192=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024