NM_014661.4(FAM53B):c.1199G>A (p.Arg400His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004217282.1
Allele description [Variation Report for NM_014661.4(FAM53B):c.1199G>A (p.Arg400His)]
NM_014661.4(FAM53B):c.1199G>A (p.Arg400His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024