ClinVar Miner

List of variants reported as uncertain significance for breast carcinoma by Leiden Open Variation Database

Included ClinVar conditions (60):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.3201+112A>G rs376034945 0.00011
NM_024675.4(PALB2):c.11C>T (p.Pro4Leu) rs45619737 0.00010
NM_024675.4(PALB2):c.1544A>G (p.Lys515Arg) rs515726072 0.00009
NM_024675.4(PALB2):c.2379C>T (p.Gly793=) rs377626805 0.00009
NM_024675.4(PALB2):c.3056T>C (p.Val1019Ala) rs376619846 0.00008
NM_024675.4(PALB2):c.2200A>T (p.Thr734Ser) rs45543843 0.00007
NM_024675.4(PALB2):c.1001A>G (p.Tyr334Cys) rs200620434 0.00006
NM_024675.4(PALB2):c.3249G>C (p.Glu1083Asp) rs147045425 0.00005
NM_024675.4(PALB2):c.1699C>T (p.His567Tyr) rs370422990 0.00004
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe) rs373478248 0.00004
NM_024675.4(PALB2):c.1756G>A (p.Asp586Asn) rs587781954 0.00003
NM_024675.4(PALB2):c.3296C>G (p.Thr1099Arg) rs142132127 0.00003
NM_024675.4(PALB2):c.3473A>G (p.His1158Arg) rs45505500 0.00003
NM_024675.4(PALB2):c.2612A>G (p.Asp871Gly) rs515726090 0.00002
NM_024675.4(PALB2):c.2903C>G (p.Ala968Gly) rs369132015 0.00002
NM_024675.4(PALB2):c.3244A>G (p.Ser1082Gly) rs786203345 0.00002
NM_024675.4(PALB2):c.3356T>C (p.Leu1119Pro) rs515726116 0.00002
NM_024675.4(PALB2):c.995T>A (p.Leu332His) rs377149139 0.00002
NM_024675.4(PALB2):c.1123C>A (p.Leu375Ile) rs373298267 0.00001
NM_024675.4(PALB2):c.1145G>T (p.Ser382Ile) rs515726063 0.00001
NM_024675.4(PALB2):c.127A>G (p.Lys43Glu) rs765125459 0.00001
NM_024675.4(PALB2):c.2514+3A>G rs515726088 0.00001
NM_024675.4(PALB2):c.2587-25A>G rs772989395 0.00001
NM_024675.4(PALB2):c.2619T>G (p.Ser873Arg) rs587782387 0.00001
NM_024675.4(PALB2):c.2792T>G (p.Leu931Arg) rs773831304 0.00001
NM_024675.4(PALB2):c.2869A>C (p.Lys957Gln) rs515726103 0.00001
NM_024675.4(PALB2):c.292A>G (p.Ile98Val) rs587782831 0.00001
NM_024675.4(PALB2):c.3128G>C (p.Gly1043Ala) rs377713277 0.00001
NM_024675.4(PALB2):c.3539T>C (p.Ile1180Thr) rs180177139 0.00001
NM_024675.4(PALB2):c.814G>A (p.Glu272Lys) rs515726127 0.00001
NM_024675.4(PALB2):c.928A>G (p.Ser310Gly) rs45561331 0.00001
NM_024675.4(PALB2):c.956C>A (p.Ser319Tyr) rs200144401 0.00001
NM_024675.4(PALB2):c.1095G>C (p.Arg365Ser) rs515726062
NM_024675.4(PALB2):c.123del (p.Glu42fs) rs1967104136
NM_024675.4(PALB2):c.1285delinsTC (p.Ile429fs) rs1966979701
NM_024675.4(PALB2):c.1475G>T (p.Gly492Val) rs515726070
NM_024675.4(PALB2):c.155T>C (p.Val52Ala) rs373970237
NM_024675.4(PALB2):c.1659C>A (p.His553Gln) rs370318597
NM_024675.4(PALB2):c.1847A>G (p.Asp616Gly) rs876660063
NM_024675.4(PALB2):c.2091C>G (p.Gly697=) rs875989797
NM_024675.4(PALB2):c.2272C>A (p.Pro758Thr) rs1064794078
NM_024675.4(PALB2):c.2418G>T (p.Pro806=) rs577076372
NM_024675.4(PALB2):c.243G>A (p.Lys81=) rs1060502775
NM_024675.4(PALB2):c.2732C>T (p.Thr911Ile) rs180177123
NM_024675.4(PALB2):c.2752C>T (p.Pro918Ser) rs515726094
NM_024675.4(PALB2):c.2834+21_2834+27del rs515726098
NM_024675.4(PALB2):c.2837C>G (p.Ala946Gly) rs515726100
NM_024675.4(PALB2):c.2865T>A (p.Ser955Arg) rs515726102
NM_024675.4(PALB2):c.3143A>G (p.Lys1048Arg) rs515726107
NM_024675.4(PALB2):c.3201+1125T>C rs515726109
NM_024675.4(PALB2):c.3287A>G (p.Asn1096Ser) rs786201142
NM_024675.4(PALB2):c.3290C>G (p.Pro1097Arg) rs587781308
NM_024675.4(PALB2):c.3306C>G (p.Ser1102Arg) rs515726112
NM_024675.4(PALB2):c.3307G>A (p.Val1103Met) rs201657283
NM_024675.4(PALB2):c.3324C>G (p.Tyr1108Ter) rs1218512317
NM_024675.4(PALB2):c.3418T>G (p.Trp1140Gly) rs62625283
NM_024675.4(PALB2):c.3428T>C (p.Leu1143Pro) rs62625284
NM_024675.4(PALB2):c.3433G>C (p.Gly1145Arg) rs180177137
NM_024675.4(PALB2):c.505C>A (p.Leu169Ile) rs180177086
NM_024675.4(PALB2):c.620C>G (p.Pro207Arg) rs515726125
NM_024675.4(PALB2):c.632A>G (p.Glu211Gly) rs180177089
NM_024675.4(PALB2):c.832C>G (p.Leu278Val) rs515726128
NM_024675.4(PALB2):c.83A>G (p.Tyr28Cys) rs515726129
NM_024675.4(PALB2):c.854C>T (p.Ser285Leu) rs180177094
NM_024675.4(PALB2):c.90G>T (p.Lys30Asn) rs515726130
NM_058216.3(RAD51C):c.180T>C (p.Thr60=) rs755092293

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