NM_004656.4(BAP1):c.1804G>C (p.Glu602Gln) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 20, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004519167.1
Allele description [Variation Report for NM_004656.4(BAP1):c.1804G>C (p.Glu602Gln)]
NM_004656.4(BAP1):c.1804G>C (p.Glu602Gln)
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
-
57471073[uid] AND (alive[prop]) (0)
Gene
-
LOC124143944 [Haliotis rufescens]
LOC124143944 [Haliotis rufescens]Gene ID:124143944Gene
-
LOC104415914 [Eucalyptus grandis]
LOC104415914 [Eucalyptus grandis]Gene ID:104415914Gene
-
LGALS8 [Camelus dromedarius]
LGALS8 [Camelus dromedarius]Gene ID:105088824Gene
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See more...Assertion and evidence details
Last Updated: May 7, 2024