NM_015695.3(BRPF3):c.562G>A (p.Val188Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004254588.1
Allele description [Variation Report for NM_015695.3(BRPF3):c.562G>A (p.Val188Ile)]
NM_015695.3(BRPF3):c.562G>A (p.Val188Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cDNA FLJ13872 fis, clone THYRO1001322
Homo sapiens cDNA FLJ13872 fis, clone THYRO1001322gi|10436027|dbj|AK023934.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024