NM_003972.3(BTAF1):c.4823A>G (p.His1608Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004191384.1
Allele description [Variation Report for NM_003972.3(BTAF1):c.4823A>G (p.His1608Arg)]
NM_003972.3(BTAF1):c.4823A>G (p.His1608Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 7, 2024