ClinVar Miner

List of variants in gene PALB2 reported as likely benign by Sema4, Sema4

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.1810C>T (p.Leu604=) rs144015319 0.00202
NM_024675.4(PALB2):c.400G>A (p.Asp134Asn) rs139555085 0.00160
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.909C>T (p.Leu303=) rs145788619 0.00101
NM_024675.4(PALB2):c.2365C>T (p.Leu789=) rs145805054 0.00099
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.1470C>T (p.Pro490=) rs45612837 0.00035
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.3054G>C (p.Glu1018Asp) rs183489969 0.00016
NM_024675.4(PALB2):c.1794G>A (p.Leu598=) rs182494675 0.00015
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.48+7G>C rs190626072 0.00013
NM_024675.4(PALB2):c.1455T>G (p.Thr485=) rs566105533 0.00011
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.1544A>G (p.Lys515Arg) rs515726072 0.00009
NM_024675.4(PALB2):c.1623G>A (p.Arg541=) rs745665968 0.00009
NM_024675.4(PALB2):c.2379C>T (p.Gly793=) rs377626805 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.1273G>A (p.Val425Met) rs576081828 0.00006
NM_024675.4(PALB2):c.1935G>A (p.Glu645=) rs141707455 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.1699C>T (p.His567Tyr) rs370422990 0.00004
NM_024675.4(PALB2):c.2067G>A (p.Ser689=) rs371149159 0.00004
NM_024675.4(PALB2):c.2082A>G (p.Thr694=) rs781440401 0.00004
NM_024675.4(PALB2):c.2289G>C (p.Leu763Phe) rs373478248 0.00004
NM_024675.4(PALB2):c.3252G>A (p.Ser1084=) rs141570833 0.00004
NM_024675.4(PALB2):c.1881G>A (p.Val627=) rs139362268 0.00003
NM_024675.4(PALB2):c.1379A>G (p.Gln460Arg) rs749494645 0.00002
NM_024675.4(PALB2):c.1743A>G (p.Leu581=) rs180177105 0.00002
NM_024675.4(PALB2):c.2253T>C (p.Ala751=) rs138514571 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.36G>A (p.Glu12=) rs760609798 0.00002
NM_024675.4(PALB2):c.807T>C (p.Gly269=) rs180177093 0.00002
NM_024675.4(PALB2):c.1164T>C (p.Pro388=) rs1205215998 0.00001
NM_024675.4(PALB2):c.1611G>A (p.Ser537=) rs730881874 0.00001
NM_024675.4(PALB2):c.1662A>G (p.Glu554=) rs786202692 0.00001
NM_024675.4(PALB2):c.2258G>A (p.Arg753Gln) rs587778586 0.00001
NM_024675.4(PALB2):c.2274C>T (p.Pro758=) rs183322618 0.00001
NM_024675.4(PALB2):c.2328C>T (p.Phe776=) rs45508997 0.00001
NM_024675.4(PALB2):c.2505C>T (p.Ser835=) rs756502783 0.00001
NM_024675.4(PALB2):c.2673C>T (p.Cys891=) rs78179744 0.00001
NM_024675.4(PALB2):c.2835-11A>G rs747232850 0.00001
NM_024675.4(PALB2):c.2955T>G (p.Ser985=) rs765643734 0.00001
NM_024675.4(PALB2):c.312T>C (p.Pro104=) rs749203259 0.00001
NM_024675.4(PALB2):c.3204G>A (p.Gly1068=) rs786203475 0.00001
NM_024675.4(PALB2):c.3276C>T (p.Leu1092=) rs779003246 0.00001
NM_024675.4(PALB2):c.3282G>A (p.Val1094=) rs747861082 0.00001
NM_024675.4(PALB2):c.660T>C (p.Ser220=) rs571762192 0.00001
NM_024675.4(PALB2):c.828C>T (p.His276=) rs911713488 0.00001
NM_024675.4(PALB2):c.834A>T (p.Leu278=) rs199919863 0.00001
NM_024675.4(PALB2):c.84C>T (p.Tyr28=) rs761533286 0.00001
NM_024675.4(PALB2):c.109-6_109-4del rs1285099815
NM_024675.4(PALB2):c.1227T>C (p.Tyr409=) rs1555461386
NM_024675.4(PALB2):c.1581T>C (p.Cys527=) rs2142411961
NM_024675.4(PALB2):c.1710G>A (p.Glu570=) rs1555460688
NM_024675.4(PALB2):c.1881G>T (p.Val627=) rs139362268
NM_024675.4(PALB2):c.1929T>C (p.Phe643=) rs995715653
NM_024675.4(PALB2):c.212-10del rs766487430
NM_024675.4(PALB2):c.2469C>G (p.Leu823=) rs515726087
NM_024675.4(PALB2):c.2490G>A (p.Glu830=) rs2142371875
NM_024675.4(PALB2):c.2592T>C (p.Pro864=) rs1597085410
NM_024675.4(PALB2):c.2802A>G (p.Val934=) rs1555459718
NM_024675.4(PALB2):c.2811A>G (p.Gly937=) rs876660486
NM_024675.4(PALB2):c.288A>C (p.Thr96=) rs878855114
NM_024675.4(PALB2):c.291T>G (p.Ser97=) rs2142446803
NM_024675.4(PALB2):c.2967A>G (p.Val989=) rs1966799199
NM_024675.4(PALB2):c.2996+9del rs769414858
NM_024675.4(PALB2):c.3027T>C (p.Pro1009=) rs876659376
NM_024675.4(PALB2):c.3474T>C (p.His1158=) rs730881896
NM_024675.4(PALB2):c.387C>T (p.Pro129=) rs1253286227
NM_024675.4(PALB2):c.525A>G (p.Arg175=) rs1555461747
NM_024675.4(PALB2):c.648T>A (p.Ile216=) rs1597098670
NM_024675.4(PALB2):c.681C>G (p.Ala227=) rs2142437477
NM_024675.4(PALB2):c.882A>G (p.Lys294=) rs1415955458
NM_024675.4(PALB2):c.957T>C (p.Ser319=) rs786203082

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