NM_001386135.1(AFF3):c.1197G>A (p.Gln399=) AND AFF3-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003952227.1
Allele description [Variation Report for NM_001386135.1(AFF3):c.1197G>A (p.Gln399=)]
NM_001386135.1(AFF3):c.1197G>A (p.Gln399=)
Condition(s)
- Name:
- AFF3-related disorder
- Synonyms:
- AFF3-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 26, 2024