ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

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Total variants: 11
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HGVS dbSNP
NM_000059.3(BRCA2):c.10176delA (p.Glu3393Asnfs) rs80359258
NM_000059.3(BRCA2):c.1744A>G (p.Thr582Ala) rs80358457
NM_000059.3(BRCA2):c.1910-6G>A rs1555282344
NM_000059.3(BRCA2):c.2484T>C (p.Tyr828=) rs45619134
NM_000059.3(BRCA2):c.3392G>A (p.Arg1131Lys) rs1555283214
NM_000059.3(BRCA2):c.4315G>A (p.Ala1439Thr) rs80358666
NM_000059.3(BRCA2):c.4928T>C (p.Val1643Ala) rs28897731
NM_000059.3(BRCA2):c.5869A>G (p.Ile1957Val) rs80358817
NM_000059.3(BRCA2):c.602C>T (p.Pro201Leu) rs397507822
NM_000059.3(BRCA2):c.6263C>T (p.Thr2088Ile) rs767567428
NM_000059.3(BRCA2):c.7056T>A (p.Pro2352=) rs276174888

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