NM_004656.4(BAP1):c.1829G>A (p.Arg610Lys) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 27, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004519170.1
Allele description [Variation Report for NM_004656.4(BAP1):c.1829G>A (p.Arg610Lys)]
NM_004656.4(BAP1):c.1829G>A (p.Arg610Lys)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
Homo sapiens E2F transcription factor 1, mRNA (cDNA clone MGC:51826 IMAGE:602505...
Homo sapiens E2F transcription factor 1, mRNA (cDNA clone MGC:51826 IMAGE:6025053), complete cdsgi|34194582|gb|BC050369.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024