ClinVar Miner

List of variants in gene PALB2 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.2851T>C (p.Ser951Pro) rs149522412 0.00058
NM_024675.4(PALB2):c.23C>T (p.Pro8Leu) rs150390726 0.00051
NM_024675.4(PALB2):c.1281T>C (p.Ala427=) rs138697796 0.00021
NM_024675.4(PALB2):c.298C>T (p.Leu100Phe) rs61756147 0.00021
NM_024675.4(PALB2):c.656A>G (p.Asp219Gly) rs45594034 0.00021
NM_024675.4(PALB2):c.2244A>G (p.Thr748=) rs750048627 0.00020
NM_024675.4(PALB2):c.1564C>T (p.Pro522Ser) rs373876101 0.00016
NM_024675.4(PALB2):c.2586+10A>G rs373321719 0.00014
NM_024675.4(PALB2):c.1641C>T (p.Thr547=) rs564514783 0.00013
NM_024675.4(PALB2):c.232G>A (p.Val78Ile) rs515726085 0.00013
NM_024675.4(PALB2):c.3257G>A (p.Arg1086Gln) rs146377793 0.00013
NM_024675.4(PALB2):c.1250C>A (p.Ser417Tyr) rs45510998 0.00011
NM_024675.4(PALB2):c.1455T>G (p.Thr485=) rs566105533 0.00011
NM_024675.4(PALB2):c.11C>T (p.Pro4Leu) rs45619737 0.00010
NM_024675.4(PALB2):c.12T>C (p.Pro4=) rs567706422 0.00009
NM_024675.4(PALB2):c.1431C>T (p.Thr477=) rs515726068 0.00009
NM_024675.4(PALB2):c.1623G>A (p.Arg541=) rs745665968 0.00009
NM_024675.4(PALB2):c.3251C>T (p.Ser1084Leu) rs62625271 0.00009
NM_024675.4(PALB2):c.344G>T (p.Gly115Val) rs145598272 0.00009
NM_024675.4(PALB2):c.3508C>T (p.His1170Tyr) rs200283306 0.00009
NM_024675.4(PALB2):c.2474G>C (p.Arg825Thr) rs146218439 0.00008
NM_024675.4(PALB2):c.2509G>A (p.Glu837Lys) rs587778587 0.00008
NM_024675.4(PALB2):c.2100A>T (p.Ser700=) rs757145884 0.00007
NM_024675.4(PALB2):c.1001A>G (p.Tyr334Cys) rs200620434 0.00006
NM_024675.4(PALB2):c.3297G>A (p.Thr1099=) rs45565738 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.3249G>C (p.Glu1083Asp) rs147045425 0.00005
NM_024675.4(PALB2):c.1699C>T (p.His567Tyr) rs370422990 0.00004
NM_024675.4(PALB2):c.194C>T (p.Pro65Leu) rs62625272 0.00004
NM_024675.4(PALB2):c.2082A>G (p.Thr694=) rs781440401 0.00004
NM_024675.4(PALB2):c.3252G>A (p.Ser1084=) rs141570833 0.00004
NM_024675.4(PALB2):c.339A>C (p.Pro113=) rs376182266 0.00004
NM_024675.4(PALB2):c.1272C>T (p.Ala424=) rs754720030 0.00003
NM_024675.4(PALB2):c.94C>G (p.Leu32Val) rs151316635 0.00003
NM_024675.4(PALB2):c.149A>C (p.Lys50Thr) rs763598472 0.00002
NM_024675.4(PALB2):c.1599T>C (p.Thr533=) rs786201088 0.00002
NM_024675.4(PALB2):c.1767G>A (p.Thr589=) rs769849072 0.00002
NM_024675.4(PALB2):c.2418G>A (p.Pro806=) rs577076372 0.00002
NM_024675.4(PALB2):c.3432C>T (p.Leu1144=) rs748363227 0.00002
NM_024675.4(PALB2):c.1119G>A (p.Glu373=) rs45623436 0.00001
NM_024675.4(PALB2):c.1188C>T (p.Cys396=) rs587780817 0.00001
NM_024675.4(PALB2):c.1311A>G (p.Lys437=) rs190489275 0.00001
NM_024675.4(PALB2):c.1446C>G (p.Leu482=) rs368759893 0.00001
NM_024675.4(PALB2):c.1569A>G (p.Ala523=) rs1200825980 0.00001
NM_024675.4(PALB2):c.1792C>T (p.Leu598=) rs746702349 0.00001
NM_024675.4(PALB2):c.1923A>G (p.Lys641=) rs775283927 0.00001
NM_024675.4(PALB2):c.1941T>C (p.His647=) rs745467835 0.00001
NM_024675.4(PALB2):c.2258G>A (p.Arg753Gln) rs587778586 0.00001
NM_024675.4(PALB2):c.2478C>T (p.Asn826=) rs786201885 0.00001
NM_024675.4(PALB2):c.2673C>T (p.Cys891=) rs78179744 0.00001
NM_024675.4(PALB2):c.2881C>T (p.Leu961=) rs61755166 0.00001
NM_024675.4(PALB2):c.351T>C (p.Pro117=) rs763330757 0.00001
NM_024675.4(PALB2):c.372C>T (p.Thr124=) rs786201904 0.00001
NM_024675.4(PALB2):c.405T>C (p.Pro135=) rs786201586 0.00001
NM_024675.4(PALB2):c.660T>C (p.Ser220=) rs571762192 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.899C>T (p.Thr300Ile) rs528541334 0.00001
NM_024675.4(PALB2):c.1093A>C (p.Arg365=) rs773001248
NM_024675.4(PALB2):c.1137G>A (p.Lys379=) rs1060504712
NM_024675.4(PALB2):c.1227T>C (p.Tyr409=) rs1555461386
NM_024675.4(PALB2):c.1758T>C (p.Asp586=) rs864622567
NM_024675.4(PALB2):c.1815T>C (p.Ser605=) rs1597091095
NM_024675.4(PALB2):c.1821C>T (p.Leu607=) rs1555460634
NM_024675.4(PALB2):c.1830A>G (p.Thr610=) rs876659484
NM_024675.4(PALB2):c.1857T>C (p.Phe619=) rs1555460623
NM_024675.4(PALB2):c.1920A>T (p.Ser640=) rs375575311
NM_024675.4(PALB2):c.2130G>A (p.Thr710=) rs774049060
NM_024675.4(PALB2):c.2469C>G (p.Leu823=) rs515726087
NM_024675.4(PALB2):c.2481A>T (p.Thr827=) rs876658885
NM_024675.4(PALB2):c.2607C>A (p.Ser869=) rs45542234
NM_024675.4(PALB2):c.2616G>T (p.Val872=) rs1567215519
NM_024675.4(PALB2):c.2715G>A (p.Gln905=) rs1555459937
NM_024675.4(PALB2):c.276T>G (p.Thr92=) rs1555461850
NM_024675.4(PALB2):c.2964A>G (p.Gln988=) rs777244673
NM_024675.4(PALB2):c.2967A>G (p.Val989=) rs1966799199
NM_024675.4(PALB2):c.2994A>G (p.Gly998=) rs2142334227
NM_024675.4(PALB2):c.3225T>C (p.Ser1075=)
NM_024675.4(PALB2):c.3307G>A (p.Val1103Met) rs201657283
NM_024675.4(PALB2):c.525A>G (p.Arg175=) rs1555461747

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