ClinVar Miner

List of variants in gene PALB2 reported as likely benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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Gene type:
ClinVar version:
Total variants: 107
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.-47G>A rs8053188 0.04991
NM_024675.4(PALB2):c.2794G>A (p.Val932Met) rs45624036 0.00449
NM_024675.4(PALB2):c.1572A>G (p.Ser524=) rs45472400 0.00312
NM_024675.4(PALB2):c.2590C>T (p.Pro864Ser) rs45568339 0.00287
NM_024675.4(PALB2):c.1810C>T (p.Leu604=) rs144015319 0.00202
NM_024675.4(PALB2):c.2256A>G (p.Gly752=) rs147120218 0.00193
NM_024675.4(PALB2):c.2742C>T (p.Phe914=) rs115759702 0.00143
NM_024675.4(PALB2):c.2816T>G (p.Leu939Trp) rs45478192 0.00121
NM_024675.4(PALB2):c.3495G>A (p.Ser1165=) rs45439097 0.00121
NM_024675.4(PALB2):c.1194G>A (p.Val398=) rs61755173 0.00103
NM_024675.4(PALB2):c.2587-38C>G rs180177119 0.00082
NM_024675.4(PALB2):c.2835-27C>T rs199757736 0.00079
NM_024675.4(PALB2):c.2996+17T>C rs180177128 0.00060
NM_024675.4(PALB2):c.2997-34A>C rs200676448 0.00058
NM_024675.4(PALB2):c.2749-18C>T rs182194007 0.00055
NM_024675.4(PALB2):c.1470C>T (p.Pro490=) rs45612837 0.00035
NM_024675.4(PALB2):c.1000T>G (p.Tyr334Asp) rs202241382 0.00026
NM_024675.4(PALB2):c.2244A>G (p.Thr748=) rs750048627 0.00020
NM_024675.4(PALB2):c.2135C>T (p.Ala712Val) rs141458731 0.00017
NM_024675.4(PALB2):c.3054G>C (p.Glu1018Asp) rs183489969 0.00016
NM_024675.4(PALB2):c.2515-46A>G rs138588349 0.00015
NM_024675.4(PALB2):c.2586+10A>G rs373321719 0.00014
NM_024675.4(PALB2):c.232G>A (p.Val78Ile) rs515726085 0.00013
NM_024675.4(PALB2):c.1250C>A (p.Ser417Tyr) rs45510998 0.00011
NM_024675.4(PALB2):c.12T>C (p.Pro4=) rs567706422 0.00009
NM_024675.4(PALB2):c.2586+30G>A rs769118926 0.00009
NM_024675.4(PALB2):c.3251C>T (p.Ser1084Leu) rs62625271 0.00009
NM_024675.4(PALB2):c.1001A>G (p.Tyr334Cys) rs200620434 0.00006
NM_024675.4(PALB2):c.1935G>A (p.Glu645=) rs141707455 0.00006
NM_024675.4(PALB2):c.3297G>A (p.Thr1099=) rs45565738 0.00006
NM_024675.4(PALB2):c.3428T>A (p.Leu1143His) rs62625284 0.00006
NM_024675.4(PALB2):c.765T>C (p.Asp255=) rs45465299 0.00006
NM_024675.4(PALB2):c.768C>T (p.Ser256=) rs45487491 0.00006
NM_024675.4(PALB2):c.2442G>A (p.Glu814=) rs140776736 0.00005
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe) rs373478248 0.00004
NM_024675.4(PALB2):c.2674G>A (p.Glu892Lys) rs45476495 0.00004
NM_024675.4(PALB2):c.3351-41G>A rs372107434 0.00004
NM_024675.4(PALB2):c.48+39C>A rs768839390 0.00004
NM_024675.4(PALB2):c.1272C>T (p.Ala424=) rs754720030 0.00003
NM_024675.4(PALB2):c.2997-28C>T rs1031537530 0.00003
NM_024675.4(PALB2):c.3113+34T>C rs201387125 0.00003
NM_024675.4(PALB2):c.3201+10G>A rs759499251 0.00003
NM_024675.4(PALB2):c.1743A>G (p.Leu581=) rs180177105 0.00002
NM_024675.4(PALB2):c.1767G>A (p.Thr589=) rs769849072 0.00002
NM_024675.4(PALB2):c.3432C>T (p.Leu1144=) rs748363227 0.00002
NM_024675.4(PALB2):c.212-45T>C rs528563270 0.00001
NM_024675.4(PALB2):c.2277A>G (p.Gln759=) rs786202524 0.00001
NM_024675.4(PALB2):c.2435C>T (p.Pro812Leu) rs774502617 0.00001
NM_024675.4(PALB2):c.2505C>T (p.Ser835=) rs756502783 0.00001
NM_024675.4(PALB2):c.2748+13C>G rs771355581 0.00001
NM_024675.4(PALB2):c.2835-11A>G rs747232850 0.00001
NM_024675.4(PALB2):c.2859T>C (p.Asp953=) rs515726101 0.00001
NM_024675.4(PALB2):c.312T>C (p.Pro104=) rs749203259 0.00001
NM_024675.4(PALB2):c.3276C>T (p.Leu1092=) rs779003246 0.00001
NM_024675.4(PALB2):c.330A>G (p.Gly110=) rs876660773 0.00001
NM_024675.4(PALB2):c.3350+11A>G rs515726114 0.00001
NM_024675.4(PALB2):c.3391A>G (p.Ile1131Val) rs774517454 0.00001
NM_024675.4(PALB2):c.48+50C>T rs1227997015 0.00001
NM_024675.4(PALB2):c.495C>T (p.Gly165=) rs200937538 0.00001
NM_024675.4(PALB2):c.546C>T (p.Ile182=) rs1597098917 0.00001
NM_024675.4(PALB2):c.78G>A (p.Arg26=) rs45572434 0.00001
NM_024675.4(PALB2):c.831C>T (p.Asp277=) rs62625273 0.00001
NM_024675.4(PALB2):c.84C>T (p.Tyr28=) rs761533286 0.00001
NM_024675.4(PALB2):c.-45C>G rs556490497
NM_024675.4(PALB2):c.108+21A>G
NM_024675.4(PALB2):c.1170T>A (p.Ser390=) rs1597096863
NM_024675.4(PALB2):c.1176A>G (p.Glu392=) rs1555461423
NM_024675.4(PALB2):c.1476G>T (p.Gly492=) rs1555461264
NM_024675.4(PALB2):c.1603A>G (p.Ser535Gly)
NM_024675.4(PALB2):c.1614T>C (p.Ile538=) rs1060504713
NM_024675.4(PALB2):c.1684+18TGA[7] rs368593832
NM_024675.4(PALB2):c.1684+18TGA[9] rs368593832
NM_024675.4(PALB2):c.1685-18C>T
NM_024675.4(PALB2):c.1685-29C>T
NM_024675.4(PALB2):c.1685-50_1685-47del rs775516114
NM_024675.4(PALB2):c.1773A>G (p.Pro591=) rs1597091237
NM_024675.4(PALB2):c.1872T>C (p.Leu624=) rs758409916
NM_024675.4(PALB2):c.2043A>G (p.Lys681=) rs1057524569
NM_024675.4(PALB2):c.211+5del rs752833998
NM_024675.4(PALB2):c.212-25T>G
NM_024675.4(PALB2):c.2469C>G (p.Leu823=) rs515726087
NM_024675.4(PALB2):c.2508C>T (p.Val836=) rs786203603
NM_024675.4(PALB2):c.2535T>C (p.Pro845=) rs1567216906
NM_024675.4(PALB2):c.2586+21C>T
NM_024675.4(PALB2):c.2586+27C>T
NM_024675.4(PALB2):c.2586+40T>C
NM_024675.4(PALB2):c.2587-24A>C
NM_024675.4(PALB2):c.2587-29C>T
NM_024675.4(PALB2):c.2587-47A>G rs2142357318
NM_024675.4(PALB2):c.2587-48A>C rs1260047262
NM_024675.4(PALB2):c.2607C>T (p.Ser869=) rs45542234
NM_024675.4(PALB2):c.2834+16G>T
NM_024675.4(PALB2):c.2834+28T>C
NM_024675.4(PALB2):c.2997-18A>T
NM_024675.4(PALB2):c.2997-44G>A
NM_024675.4(PALB2):c.3054G>T (p.Glu1018Asp) rs183489969
NM_024675.4(PALB2):c.3201+36A>G
NM_024675.4(PALB2):c.3202-20T>C
NM_024675.4(PALB2):c.3202-34T>C
NM_024675.4(PALB2):c.3285T>A (p.Ile1095=)
NM_024675.4(PALB2):c.3287A>C (p.Asn1096Thr)
NM_024675.4(PALB2):c.3293A>C (p.Lys1098Thr)
NM_024675.4(PALB2):c.3350+39C>G rs568248665
NM_024675.4(PALB2):c.3438G>A (p.Gln1146=)
NM_024675.4(PALB2):c.48+26C>A
NM_024675.4(PALB2):c.48+29A>G
NM_024675.4(PALB2):c.792C>T (p.His264=) rs1310569612

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