ClinVar Miner

List of variants studied for Fanconi anemia complementation group N; Pancreatic cancer, susceptibility to, 3; Breast-ovarian cancer, familial, susceptibility to, 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_024675.4(PALB2):c.3257G>A (p.Arg1086Gln) rs146377793 0.00013
NM_024675.4(PALB2):c.3412G>A (p.Ala1138Thr) rs577651839 0.00005
NM_024675.4(PALB2):c.2674G>A (p.Glu892Lys) rs45476495 0.00004
NM_024675.4(PALB2):c.226A>G (p.Ile76Val) rs541028076 0.00003
NM_024675.4(PALB2):c.3035C>T (p.Thr1012Ile) rs761032954 0.00003
NM_024675.4(PALB2):c.788A>G (p.Glu263Gly) rs745553724 0.00003
NM_024675.4(PALB2):c.94C>G (p.Leu32Val) rs151316635 0.00003
NM_024675.4(PALB2):c.2755G>A (p.Val919Ile) rs775193384 0.00002
NM_024675.4(PALB2):c.2840T>C (p.Leu947Ser) rs45464500 0.00002
NM_024675.4(PALB2):c.3113G>A (p.Trp1038Ter) rs180177132 0.00002
NM_024675.4(PALB2):c.3256C>T (p.Arg1086Ter) rs587776527 0.00002
NM_024675.4(PALB2):c.3356T>C (p.Leu1119Pro) rs515726116 0.00002
NM_024675.4(PALB2):c.1052C>A (p.Thr351Lys) rs876658656 0.00001
NM_024675.4(PALB2):c.1240C>T (p.Arg414Ter) rs180177100 0.00001
NM_024675.4(PALB2):c.1361C>T (p.Ser454Phe) rs587782842 0.00001
NM_024675.4(PALB2):c.1697G>A (p.Arg566His) rs144617793 0.00001
NM_024675.4(PALB2):c.196C>T (p.Gln66Ter) rs180177083 0.00001
NM_024675.4(PALB2):c.206A>T (p.His69Leu) rs749443090 0.00001
NM_024675.4(PALB2):c.2087C>T (p.Thr696Met) rs587780820 0.00001
NM_024675.4(PALB2):c.2167A>T (p.Met723Leu) rs876660336 0.00001
NM_024675.4(PALB2):c.2514+3A>G rs515726088 0.00001
NM_024675.4(PALB2):c.2606C>T (p.Ser869Phe) rs779279139 0.00001
NM_024675.4(PALB2):c.2821A>G (p.Ile941Val) rs778602038 0.00001
NM_024675.4(PALB2):c.2846G>A (p.Cys949Tyr) rs587778588 0.00001
NM_024675.4(PALB2):c.303T>G (p.Asp101Glu) rs1417779335 0.00001
NM_024675.4(PALB2):c.3113+5G>C rs876659463 0.00001
NM_024675.4(PALB2):c.3379T>C (p.Cys1127Arg) rs767830005 0.00001
NM_024675.4(PALB2):c.3518C>T (p.Ala1173Val) rs146659762 0.00001
NM_024675.4(PALB2):c.833T>A (p.Leu278Gln) rs200843485 0.00001
NM_024675.4(PALB2):c.109-2A>G rs730881897
NM_024675.4(PALB2):c.1183del (p.Ser395fs) rs1555461415
NM_024675.4(PALB2):c.1252A>G (p.Asn418Asp) rs786202943
NM_024675.4(PALB2):c.1429A>G (p.Thr477Ala) rs1555461285
NM_024675.4(PALB2):c.1687A>G (p.Lys563Glu)
NM_024675.4(PALB2):c.1694G>T (p.Ser565Ile) rs876659914
NM_024675.4(PALB2):c.1748T>C (p.Leu583Ser) rs587782151
NM_024675.4(PALB2):c.184G>T (p.Asp62Tyr)
NM_024675.4(PALB2):c.1919C>A (p.Ser640Ter) rs760094988
NM_024675.4(PALB2):c.1924del (p.Met642fs) rs730881865
NM_024675.4(PALB2):c.2495A>G (p.His832Arg)
NM_024675.4(PALB2):c.2504C>G (p.Ser835Cys)
NM_024675.4(PALB2):c.2506G>A (p.Val836Ile) rs536644825
NM_024675.4(PALB2):c.2507_2509del (p.Val836del) rs587782697
NM_024675.4(PALB2):c.2748+1G>A rs753153576
NM_024675.4(PALB2):c.2835-1G>C rs515726099
NM_024675.4(PALB2):c.2897T>A (p.Ile966Lys) rs587780214
NM_024675.4(PALB2):c.2938del (p.Ser980fs) rs1555459540
NM_024675.4(PALB2):c.3047T>G (p.Phe1016Cys) rs879254154
NM_024675.4(PALB2):c.3048T>G (p.Phe1016Leu) rs1567212918
NM_024675.4(PALB2):c.3087del (p.Thr1030fs)
NM_024675.4(PALB2):c.3306C>G (p.Ser1102Arg) rs515726112
NM_024675.4(PALB2):c.3351-1G>A rs1597062406
NM_024675.4(PALB2):c.3441T>A (p.Cys1147Ter) rs1555457867
NM_024675.4(PALB2):c.3500C>T (p.Thr1167Ile) rs1308784980
NM_024675.4(PALB2):c.3507_3508del (p.His1170fs) rs587776428
NM_024675.4(PALB2):c.398G>T (p.Ser133Ile) rs864622411
NM_024675.4(PALB2):c.583A>G (p.Ile195Val) rs760784181
NM_024675.4(PALB2):c.71_73delinsGG (p.Leu24fs) rs1967112121
NM_024675.4(PALB2):c.72del (p.Arg26fs) rs180177142
NM_024675.4(PALB2):c.892_893del (p.Val298fs) rs2142431841
NM_024675.4:c.3179_3180insALU

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