ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.3262C>T (p.Pro1088Ser) rs80358572 0.00009
NM_000059.4(BRCA2):c.7601C>T (p.Ala2534Val) rs74047012 0.00009
NM_000059.4(BRCA2):c.9501+3A>T rs61757642 0.00008
NM_000059.4(BRCA2):c.3539A>G (p.Lys1180Arg) rs28897720 0.00005
NM_000059.4(BRCA2):c.136C>T (p.Pro46Ser) rs80358425 0.00004
NM_000059.4(BRCA2):c.3032C>G (p.Thr1011Arg) rs80358548 0.00004
NM_000059.4(BRCA2):c.5869A>G (p.Ile1957Val) rs80358817 0.00004
NM_000059.4(BRCA2):c.1012G>A (p.Ala338Thr) rs80358396 0.00003
NM_000059.4(BRCA2):c.10202C>T (p.Thr3401Met) rs55853199 0.00002
NM_000059.4(BRCA2):c.4178C>T (p.Ala1393Val) rs398122776 0.00002
NM_000059.4(BRCA2):c.8111C>T (p.Ser2704Phe) rs80359054 0.00002
NM_000059.4(BRCA2):c.8687G>A (p.Arg2896His) rs80359128 0.00002
NM_000059.4(BRCA2):c.4315G>A (p.Ala1439Thr) rs80358666 0.00001
NM_000059.4(BRCA2):c.5870T>C (p.Ile1957Thr) rs587782320 0.00001
NM_000059.4(BRCA2):c.6115T>A (p.Leu2039Ile) rs370026879 0.00001
NM_000059.4(BRCA2):c.6263C>T (p.Thr2088Ile) rs767567428 0.00001
NM_000059.4(BRCA2):c.6458C>T (p.Pro2153Leu) rs276174873 0.00001
NM_000059.4(BRCA2):c.6467C>T (p.Ser2156Phe) rs765575482 0.00001
NM_000059.4(BRCA2):c.7055C>T (p.Pro2352Leu) rs80358934 0.00001
NM_000059.4(BRCA2):c.7448G>A (p.Ser2483Asn) rs80358967 0.00001
NM_000059.4(BRCA2):c.8416T>C (p.Ser2806Pro) rs1280487930 0.00001
NM_000059.4(BRCA2):c.9689T>C (p.Leu3230Ser) rs1476814134 0.00001
NM_000059.4(BRCA2):c.10176del (p.Glu3393fs) rs80359258
NM_000059.4(BRCA2):c.121C>T (p.Pro41Ser) rs80358415
NM_000059.4(BRCA2):c.1616G>A (p.Gly539Glu)
NM_000059.4(BRCA2):c.1627C>A (p.His543Asn) rs80358446
NM_000059.4(BRCA2):c.1661G>A (p.Cys554Tyr) rs748215651
NM_000059.4(BRCA2):c.1744A>G (p.Thr582Ala) rs80358457
NM_000059.4(BRCA2):c.1910-6G>A rs1555282344
NM_000059.4(BRCA2):c.2187A>G (p.Ile729Met) rs397507620
NM_000059.4(BRCA2):c.2553C>A (p.Phe851Leu)
NM_000059.4(BRCA2):c.2921A>G (p.Asp974Gly) rs2137491259
NM_000059.4(BRCA2):c.3392G>A (p.Arg1131Lys) rs1555283214
NM_000059.4(BRCA2):c.3446T>C (p.Met1149Thr) rs80358590
NM_000059.4(BRCA2):c.4058A>C (p.Glu1353Ala) rs2137502526
NM_000059.4(BRCA2):c.426-12_426-8del rs276174844
NM_000059.4(BRCA2):c.5444C>T (p.Thr1815Ile) rs587782031
NM_000059.4(BRCA2):c.5479A>G (p.Ile1827Val) rs80358770
NM_000059.4(BRCA2):c.5678G>A (p.Cys1893Tyr) rs2072535635
NM_000059.4(BRCA2):c.602C>T (p.Pro201Leu) rs397507822
NM_000059.4(BRCA2):c.6080G>A (p.Arg2027Lys) rs431825337
NM_000059.4(BRCA2):c.622G>C (p.Val208Leu) rs1593887544
NM_000059.4(BRCA2):c.6347A>T (p.His2116Leu) rs55953736
NM_000059.4(BRCA2):c.6523G>C (p.Glu2175Gln) rs876658412
NM_000059.4(BRCA2):c.6533_6538del (p.His2178_Val2179del) rs2137528401
NM_000059.4(BRCA2):c.673ACT[1] (p.Thr226del) rs1566220661
NM_000059.4(BRCA2):c.6931C>A (p.Pro2311Thr) rs730881551
NM_000059.4(BRCA2):c.7056T>A (p.Pro2352=) rs276174888
NM_000059.4(BRCA2):c.7069C>G (p.Leu2357Val) rs1316815571
NM_000059.4(BRCA2):c.7417T>C (p.Cys2473Arg) rs786202720
NM_000059.4(BRCA2):c.7661G>A (p.Ser2554Asn) rs398122588
NM_000059.4(BRCA2):c.7977-4_7977-3del rs876659992
NM_000059.4(BRCA2):c.7977-5T>C rs1593924692
NM_000059.4(BRCA2):c.8141A>G (p.Gln2714Arg) rs80359059
NM_000059.4(BRCA2):c.8181_8189del (p.Val2728_Ala2730del) rs786203465
NM_000059.4(BRCA2):c.8775G>C (p.Gln2925His) rs80359136
NM_000059.4(BRCA2):c.9104A>G (p.Tyr3035Cys) rs80359165
NM_000059.4(BRCA2):c.9172A>G (p.Ser3058Gly) rs80359173
NM_000059.4(BRCA2):c.9613_9614delinsCT (p.Ala3205Leu) rs276174926
NM_000059.4(BRCA2):c.9619A>T (p.Ile3207Phe) rs1057520802

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