ClinVar Miner

List of variants in gene BRCA2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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Gene type:
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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.9501+3A>T rs61757642 0.00008
NM_000059.4(BRCA2):c.257T>C (p.Leu86Pro) rs572782576 0.00007
NM_000059.4(BRCA2):c.2957A>G (p.Asn986Ser) rs28897718 0.00006
NM_000059.4(BRCA2):c.3073A>G (p.Lys1025Glu) rs80358550 0.00006
NM_000059.4(BRCA2):c.9454G>A (p.Glu3152Lys) rs80359218 0.00006
NM_000059.4(BRCA2):c.9353T>C (p.Met3118Thr) rs56204128 0.00005
NM_000059.4(BRCA2):c.6290C>T (p.Thr2097Met) rs80358866 0.00004
NM_000059.4(BRCA2):c.887A>G (p.Tyr296Cys) rs45457795 0.00004
NM_000059.4(BRCA2):c.3417G>T (p.Lys1139Asn) rs145625991 0.00003
NM_000059.4(BRCA2):c.9190G>A (p.Asp3064Asn) rs80359177 0.00003
NM_000059.4(BRCA2):c.10089A>G (p.Ile3363Met) rs80358390 0.00002
NM_000059.4(BRCA2):c.2944A>C (p.Ile982Leu) rs28897717 0.00002
NM_000059.4(BRCA2):c.5737T>C (p.Cys1913Arg) rs80358799 0.00002
NM_000059.4(BRCA2):c.10085T>C (p.Phe3362Ser) rs756978580 0.00001
NM_000059.4(BRCA2):c.1397A>G (p.Asn466Ser) rs370692951 0.00001
NM_000059.4(BRCA2):c.1466C>G (p.Ser489Cys) rs587782535 0.00001
NM_000059.4(BRCA2):c.2026T>C (p.Cys676Arg) rs397507280 0.00001
NM_000059.4(BRCA2):c.215A>G (p.Asn72Ser) rs276174818 0.00001
NM_000059.4(BRCA2):c.4271C>G (p.Ser1424Cys) rs80358664 0.00001
NM_000059.4(BRCA2):c.5272A>G (p.Asn1758Asp) rs80358750 0.00001
NM_000059.4(BRCA2):c.5663A>G (p.Lys1888Arg) rs80358791 0.00001
NM_000059.4(BRCA2):c.5884A>G (p.Ile1962Val) rs747406932 0.00001
NM_000059.4(BRCA2):c.7429C>A (p.Pro2477Thr) rs80358964 0.00001
NM_000059.4(BRCA2):c.7540A>G (p.Lys2514Glu) rs864622624 0.00001
NM_000059.4(BRCA2):c.793+6T>C rs1222477192 0.00001
NM_000059.4(BRCA2):c.7992T>A (p.Ile2664=) rs80359800 0.00001
NM_000059.4(BRCA2):c.825A>T (p.Lys275Asn) rs397507399 0.00001
NM_000059.4(BRCA2):c.8356G>A (p.Ala2786Thr) rs80359077 0.00001
NM_000059.4(BRCA2):c.8435G>A (p.Gly2812Glu) rs80359091 0.00001
NM_000059.4(BRCA2):c.10095delinsGAATTATATCT (p.Ser3366fs) rs276174803
NM_000059.4(BRCA2):c.1709A>G (p.Asn570Ser) rs431825284
NM_000059.4(BRCA2):c.277T>G (p.Ser93Ala) rs776730435
NM_000059.4(BRCA2):c.3070A>G (p.Ile1024Val) rs876659687
NM_000059.4(BRCA2):c.3343T>C (p.Ser1115Pro) rs1204868565
NM_000059.4(BRCA2):c.3721T>C (p.Phe1241Leu) rs2137499348
NM_000059.4(BRCA2):c.3800A>G (p.Asp1267Gly) rs1555283400
NM_000059.4(BRCA2):c.3858A>T (p.Lys1286Asn) rs1555283430
NM_000059.4(BRCA2):c.3858_3860del (p.Lys1286del) rs80359406
NM_000059.4(BRCA2):c.4045A>G (p.Ile1349Val) rs780544697
NM_000059.4(BRCA2):c.5554G>A (p.Val1852Ile) rs80358777
NM_000059.4(BRCA2):c.5837C>T (p.Ser1946Leu) rs2137521516
NM_000059.4(BRCA2):c.7007+5G>A rs81002816
NM_000059.4(BRCA2):c.7154T>G (p.Val2385Gly) rs1555286021
NM_000059.4(BRCA2):c.7630G>A (p.Gly2544Ser) rs587781485
NM_000059.4(BRCA2):c.8128A>G (p.Ser2710Gly) rs398122597
NM_000059.4(BRCA2):c.865A>G (p.Asn289Asp) rs766173
NM_000059.4(BRCA2):c.9816T>G (p.Asp3272Glu) rs56111359

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