NM_000059.4(BRCA2):c.68-17A>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 24, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000581854.3
Allele description [Variation Report for NM_000059.4(BRCA2):c.68-17A>G]
NM_000059.4(BRCA2):c.68-17A>G
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
-
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UDP-glycosyltransferase 72E1-like [Raphanus sativus]gi|2515517779|ref|XP_018470156.2|Protein
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Megastigmus hoffmeyeri isolate Mhof.CAN cytochrome b (cytb) gene, partial cds; m...
Megastigmus hoffmeyeri isolate Mhof.CAN cytochrome b (cytb) gene, partial cds; mitochondrialgi|60250702|gb|AY898695.1|Nucleotide
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Schwannoma of ureter
Schwannoma of ureterMedGen
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024