ClinVar Miner

List of variants reported as benign for pancreatic neoplasm

Included ClinVar conditions (36):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 122
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HGVS dbSNP gnomAD frequency
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) rs1042522 0.62654
NM_001166108.2(PALLD):c.*2058C>G rs1071738 0.51499
NM_001166108.2(PALLD):c.1964+44318A>G rs12510359 0.50401
NM_001166108.2(PALLD):c.1965-12625A>G rs62333013 0.49745
NM_001166108.2(PALLD):c.-161A>T rs2710836 0.33669
NM_007294.4(BRCA1):c.2082C>T (p.Ser694=) rs1799949 0.30810
NM_007294.4(BRCA1):c.3548A>G (p.Lys1183Arg) rs16942 0.30784
NM_001166108.2(PALLD):c.671T>C (p.Met224Thr) rs7655494 0.29609
NM_001166108.2(PALLD):c.678C>T (p.Asp226=) rs7673220 0.29605
NM_001166108.2(PALLD):c.672G>A (p.Met224Ile) rs7671781 0.29602
NM_001166108.2(PALLD):c.186G>A (p.Lys62=) rs1806729 0.29323
NM_007294.4(BRCA1):c.4308T>C (p.Ser1436=) rs1060915 0.29170
NM_007294.4(BRCA1):c.3113A>G (p.Glu1038Gly) rs16941 0.29115
NM_007294.4(BRCA1):c.2311T>C (p.Leu771=) rs16940 0.29035
NM_000059.4(BRCA2):c.1114A>C (p.Asn372His) rs144848 0.23116
NM_001166108.2(PALLD):c.18C>T (p.Ser6=) rs61051061 0.21059
NM_001166108.2(PALLD):c.*1906G>A rs1136603 0.13125
NM_024675.4(PALB2):c.1676A>G (p.Gln559Arg) rs152451 0.12980
NM_001166108.2(PALLD):c.2679A>G (p.Arg893=) rs1059444 0.12743
NM_001166108.2(PALLD):c.1274C>A (p.Thr425Asn) rs62333891 0.12308
NM_001166108.2(PALLD):c.789C>T (p.Ser263=) rs72695199 0.09674
NM_007294.4(BRCA1):c.2077G>A (p.Asp693Asn) rs4986850 0.05782
NM_007294.4(BRCA1):c.1067A>G (p.Gln356Arg) rs1799950 0.04695
NM_000059.4(BRCA2):c.2971A>G (p.Asn991Asp) rs1799944 0.04357
NM_001166108.2(PALLD):c.1347C>T (p.Asn449=) rs17054482 0.03942
NM_000059.4(BRCA2):c.10234A>G (p.Ile3412Val) rs1801426 0.03864
NM_000059.4(BRCA2):c.2229T>C (p.His743=) rs1801499 0.03698
NM_000059.4(BRCA2):c.865A>C (p.Asn289His) rs766173 0.03693
NM_001166108.2(PALLD):c.1527T>G (p.Ala509=) rs58395080 0.02196
NM_001166108.2(PALLD):c.3359-4G>A rs112116419 0.01852
NM_000059.4(BRCA2):c.8830A>T (p.Ile2944Phe) rs4987047 0.01281
NM_001166108.2(PALLD):c.*992A>G rs28718025 0.01242
NM_001166108.2(PALLD):c.*1164T>G rs114351964 0.01238
NM_000059.4(BRCA2):c.8460A>C (p.Val2820=) rs9590940 0.01220
NM_007294.4(BRCA1):c.3119G>A (p.Ser1040Asn) rs4986852 0.01109
NM_000059.4(BRCA2):c.7319A>G (p.His2440Arg) rs4986860 0.00984
NM_007294.4(BRCA1):c.2458A>G (p.Lys820Glu) rs56082113 0.00964
NM_000059.4(BRCA2):c.7469T>C (p.Ile2490Thr) rs11571707 0.00868
NM_000059.4(BRCA2):c.7017G>C (p.Lys2339Asn) rs45574331 0.00792
NM_000059.4(BRCA2):c.9730G>A (p.Val3244Ile) rs11571831 0.00792
NM_000059.4(BRCA2):c.5418A>G (p.Glu1806=) rs34351119 0.00791
NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=) rs114593924 0.00564
NM_001166108.2(PALLD):c.1965-12953C>T rs528879194 0.00493
NM_007294.4(BRCA1):c.5468-10C>A rs8176316 0.00464
NM_024675.4(PALB2):c.2794G>A (p.Val932Met) rs45624036 0.00449
NM_000059.4(BRCA2):c.7008-62A>G rs76584943 0.00439
NM_001166108.2(PALLD):c.-83+8A>G rs143268375 0.00367
NM_001166108.2(PALLD):c.1273A>T (p.Thr425Ser) rs140454899 0.00299
NM_001166108.2(PALLD):c.502C>G (p.Leu168Val) rs115607645 0.00299
NM_001166108.2(PALLD):c.764G>A (p.Arg255His) rs146018183 0.00287
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile) rs1800744 0.00240
NM_000059.4(BRCA2):c.3516G>A (p.Ser1172=) rs1799952 0.00228
NM_001166108.2(PALLD):c.*492A>G rs113794451 0.00224
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00218
NM_000059.4(BRCA2):c.231T>G (p.Thr77=) rs114446594 0.00191
NM_001166108.2(PALLD):c.731A>G (p.Gln244Arg) rs114946738 0.00143
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp) rs1800709 0.00137
NM_000546.6(TP53):c.139C>T (p.Pro47Ser) rs1800371 0.00123
NM_001166108.2(PALLD):c.1394G>A (p.Arg465His) rs115372194 0.00111
NM_001166108.2(PALLD):c.1965-12665G>C rs535155432 0.00111
NM_001166108.2(PALLD):c.909A>T (p.Arg303Ser) rs138897963 0.00108
NM_001166108.2(PALLD):c.33-4G>A rs113515140 0.00105
NM_001166108.2(PALLD):c.*1594T>C rs148023504 0.00102
NM_001166108.2(PALLD):c.1849C>T (p.Arg617Cys) rs138283237 0.00102
NM_001166108.2(PALLD):c.1965-12594T>G rs587780760 0.00102
NM_001166108.2(PALLD):c.2393T>C (p.Met798Thr) rs142116575 0.00102
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=) rs59633770 0.00098
NM_001166108.2(PALLD):c.*946C>A rs76997292 0.00096
NM_001166108.2(PALLD):c.-179G>C rs540595354 0.00088
NM_001166108.2(PALLD):c.2199+8G>A rs200060953 0.00070
NM_001166108.2(PALLD):c.1040C>T (p.Thr347Met) rs150711066 0.00065
NM_001166108.2(PALLD):c.365C>T (p.Pro122Leu) rs116158771 0.00064
NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro) rs56119278 0.00059
NM_001166108.2(PALLD):c.*1829T>C rs184106989 0.00046
NM_001166108.2(PALLD):c.1965-12910C>G rs550499593 0.00046
NM_001166108.2(PALLD):c.2748C>T (p.Asp916=) rs143544548 0.00039
NM_001166108.2(PALLD):c.8G>T (p.Gly3Val) rs189385916 0.00036
NM_001166108.2(PALLD):c.2892T>C (p.Asp964=) rs140584890 0.00028
NM_000059.4(BRCA2):c.5070A>C (p.Lys1690Asn) rs56087561 0.00023
NM_001166108.2(PALLD):c.1965-10T>A rs149239490 0.00022
NM_001166108.2(PALLD):c.1965-12840C>G rs587780757 0.00020
NM_007294.4(BRCA1):c.4484+14A>G rs80358022 0.00019
NM_001166108.2(PALLD):c.2472+13A>G rs190608408 0.00018
NM_007294.4(BRCA1):c.5406+33A>T rs80358092 0.00018
NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln) rs145571230 0.00016
NM_007294.4(BRCA1):c.3296C>T (p.Pro1099Leu) rs80357201 0.00016
NM_001166108.2(PALLD):c.*994A>G rs185646548 0.00014
NM_001166108.2(PALLD):c.1965-13016C>T rs561750970 0.00013
NM_001166108.2(PALLD):c.195G>A (p.Ser65=) rs369178136 0.00011
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys) rs41286300 0.00011
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=) rs114250766 0.00010
NM_001166108.2(PALLD):c.1965-12530C>T rs753092219 0.00009
NM_001166108.2(PALLD):c.453C>T (p.Asn151=) rs143682790 0.00009
NM_000059.4(BRCA2):c.9501+3A>T rs61757642 0.00008
NM_001166108.2(PALLD):c.-8G>A rs372273201 0.00006
NM_001166108.2(PALLD):c.2084T>G (p.Leu695Arg) rs139375029 0.00006
NM_001166108.2(PALLD):c.1965-12565G>A rs368350042 0.00004
NM_001166108.2(PALLD):c.556G>A (p.Ala186Thr) rs139434937 0.00003
NM_001166108.2(PALLD):c.1872C>T (p.Asn624=) rs189427176 0.00002
NM_001166108.2(PALLD):c.*2214C>T rs145960760 0.00001
NM_001166108.2(PALLD):c.65A>G (p.Lys22Arg) rs201343910 0.00001
NM_001166108.2(PALLD):c.*1132T>C rs575893643
NM_001166108.2(PALLD):c.*2156del rs398064261
NM_001166108.2(PALLD):c.*2162ATCA[2] rs71719276
NM_001166108.2(PALLD):c.*325del rs796761323
NM_001166108.2(PALLD):c.-162C>T rs538959058
NM_001166108.2(PALLD):c.1965-12688CCG[3] rs200020758
NM_001166108.2(PALLD):c.1965-12693_1965-12692insCCC
NM_001166108.2(PALLD):c.1965-12694CCA[3] rs201979617
NM_001166108.2(PALLD):c.1965-12701GCC[4] rs748729107
NM_001166108.2(PALLD):c.1965-12736A>C rs864622226
NM_001166108.2(PALLD):c.1965-12755A>C rs863224385
NM_001166108.2(PALLD):c.1965-12758G>C rs777359545
NM_001166108.2(PALLD):c.1965-12764G>C rs863224384
NM_001166108.2(PALLD):c.1965-12771CGCCCC[3] rs730882137
NM_001166108.2(PALLD):c.2199+5del rs376654786
NM_001166108.2(PALLD):c.3059-6del rs755470870
NM_001166108.2(PALLD):c.3150A>G (p.Val1050=) rs781516286
NM_001166108.2(PALLD):c.671_672inv (p.Met224Thr) rs373066707
NM_007294.4(BRCA1):c.2612C>T (p.Pro871Leu) rs799917
NM_007294.4(BRCA1):c.441+36_441+49del rs373413425
NM_007294.4(BRCA1):c.4837A>G (p.Ser1613Gly) rs1799966

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