ClinVar Miner

List of variants in gene BRCA2 reported as pathogenic for Neoplasm of the breast

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Gene type:
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Total variants: 49
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HGVS dbSNP
NM_000059.3(BRCA2):c.-7_9del16 rs1555280073
NM_000059.3(BRCA2):c.1190_1197del (p.Gln397Profs) rs886037797
NM_000059.3(BRCA2):c.1399A>T (p.Lys467Ter) rs80358427
NM_000059.3(BRCA2):c.161delA (p.Asn54Thrfs) rs878853297
NM_000059.3(BRCA2):c.2059_2063delGATTA (p.Asp687Terfs) rs587782780
NM_000059.3(BRCA2):c.2095C>T (p.Gln699Ter) rs878853559
NM_000059.3(BRCA2):c.2175dupA (p.Val726Serfs) rs276174819
NM_000059.3(BRCA2):c.2266C>T (p.Gln756Ter) rs1057518637
NM_000059.3(BRCA2):c.2595delA (p.Glu866Lysfs) rs483353111
NM_000059.3(BRCA2):c.274C>T (p.Gln92Ter) rs80358529
NM_000059.3(BRCA2):c.2754delC (p.Asn918Lysfs) rs1555282830
NM_000059.3(BRCA2):c.2808_2811del (p.Ala938Profs) rs80359351
NM_000059.3(BRCA2):c.2828_2831delTTAA (p.Ile943Lysfs) rs397507643
NM_000059.3(BRCA2):c.2845delT (p.Tyr949Metfs) rs397507644
NM_000059.3(BRCA2):c.2990T>G (p.Leu997Ter) rs397507649
NM_000059.3(BRCA2):c.3001del (p.Ser1001Glnfs) rs886037801
NM_000059.3(BRCA2):c.3322A>T (p.Lys1108Ter) rs1555283169
NM_000059.3(BRCA2):c.3834_3835delTA (p.His1278Glnfs) rs886037803
NM_000059.3(BRCA2):c.3883C>T (p.Gln1295Ter) rs879255309
NM_000059.3(BRCA2):c.4041_4042del (p.Cys1348Tyrfs) rs886037800
NM_000059.3(BRCA2):c.4148_4149delAT (p.Asp1383Valfs) rs886037799
NM_000059.3(BRCA2):c.4151delT (p.Leu1384Cysfs) rs397507710
NM_000059.3(BRCA2):c.4740_4741dupTG (p.Glu1581Valfs) rs864622401
NM_000059.3(BRCA2):c.4962T>A (p.Cys1654Ter) rs1057518638
NM_000059.3(BRCA2):c.5206C>T (p.Gln1736Ter) rs886037802
NM_000059.3(BRCA2):c.5645C>A (p.Ser1882Ter) rs80358785
NM_000059.3(BRCA2):c.5879del (p.Cys1960Leufs) rs1555284442
NM_000059.3(BRCA2):c.5946delT (p.Ser1982Argfs) rs80359550
NM_000059.3(BRCA2):c.6014_6017delATAG (p.Asp2005Valfs) rs1057518635
NM_000059.3(BRCA2):c.6085G>T (p.Glu2029Ter) rs397507828
NM_000059.3(BRCA2):c.6405_6409delCTTAA (p.Asn2135Lysfs) rs80359584
NM_000059.3(BRCA2):c.6532dupC (p.His2178Profs) rs886037798
NM_000059.3(BRCA2):c.6553delG (p.Ala2185Leufs) rs80359603
NM_000059.3(BRCA2):c.67+1G>C rs81002796
NM_000059.3(BRCA2):c.6952C>T (p.Arg2318Ter) rs80358920
NM_000059.3(BRCA2):c.7558C>T (p.Arg2520Ter) rs80358981
NM_000059.3(BRCA2):c.800dup (p.Thr269Asnfs) rs1555281594
NM_000059.3(BRCA2):c.8195T>G (p.Leu2732Ter) rs397507967
NM_000059.3(BRCA2):c.8203delC (p.Leu2736Serfs) rs397507396
NM_000059.3(BRCA2):c.8322dupT (p.Met2775Tyrfs) rs80359706
NM_000059.3(BRCA2):c.8400_8402delTTTinsAAAA (p.Phe2801Lysfs) rs483353077
NM_000059.3(BRCA2):c.857C>G (p.Ser286Ter) rs1131692035
NM_000059.3(BRCA2):c.8633_8755del
NM_000059.3(BRCA2):c.9011delA (p.Lys3004Argfs) rs886037804
NM_000059.3(BRCA2):c.9318G>A (p.Trp3106Ter) rs771203198
NM_000059.3(BRCA2):c.9382C>T (p.Arg3128Ter) rs80359212
NM_000059.3(BRCA2):c.9401delG (p.Gly3134Alafs) rs80359759
NM_000059.3(BRCA2):c.9481A>T (p.Lys3161Ter) rs80359222
NM_000059.3(BRCA2):c.9753delG (p.Lys3251Asnfs) rs886037805

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