NM_001003694.2(BRPF1):c.1209C>T (p.Ala403=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000920787.5
Allele description [Variation Report for NM_001003694.2(BRPF1):c.1209C>T (p.Ala403=)]
NM_001003694.2(BRPF1):c.1209C>T (p.Ala403=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC127891821 [Homo sapiens]
LOC127891821 [Homo sapiens]Gene ID:127891821Gene
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Last Updated: Sep 29, 2024