NM_032043.3(BRIP1):c.919-8G>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001188605.3
Allele description [Variation Report for NM_032043.3(BRIP1):c.919-8G>T]
NM_032043.3(BRIP1):c.919-8G>T
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 unk like zinc finger (UNKL), transcript variant 5, mRNA
Homo sapiens unk like zinc finger (UNKL), transcript variant 5, mRNAgi|1635577158|ref|NM_001276414.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024