ClinVar Miner

List of variants reported as benign for exocrine pancreatic carcinoma by Illumina Laboratory Services, Illumina

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.*2058C>G rs1071738 0.51499
NM_001166108.2(PALLD):c.-161A>T rs2710836 0.33669
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_001166108.2(PALLD):c.18C>T (p.Ser6=) rs61051061 0.21059
NM_001166108.2(PALLD):c.*1906G>A rs1136603 0.13125
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_001166108.2(PALLD):c.1347C>T (p.Asn449=) rs17054482 0.03942
NM_001166108.2(PALLD):c.1527T>G (p.Ala509=) rs58395080 0.02196
NM_001166108.2(PALLD):c.3359-4G>A rs112116419 0.01852
NM_001166108.2(PALLD):c.*992A>G rs28718025 0.01242
NM_001166108.2(PALLD):c.*1164T>G rs114351964 0.01238
NM_001166108.2(PALLD):c.3297T>C (p.Tyr1099=) rs114593924 0.00564
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_001166108.2(PALLD):c.*492A>G rs113794451 0.00224
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00218
NM_001166108.2(PALLD):c.731A>G (p.Gln244Arg) rs114946738 0.00143
NM_001166108.2(PALLD):c.1394G>A (p.Arg465His) rs115372194 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.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.1040C>T (p.Thr347Met) rs150711066 0.00065
NM_001166108.2(PALLD):c.365C>T (p.Pro122Leu) rs116158771 0.00064
NM_001166108.2(PALLD):c.*1829T>C rs184106989 0.00046
NM_001166108.2(PALLD):c.8G>T (p.Gly3Val) rs189385916 0.00036
NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln) rs145571230 0.00016
NM_001166108.2(PALLD):c.*994A>G rs185646548 0.00014
NM_001166108.2(PALLD):c.195G>A (p.Ser65=) rs369178136 0.00011
NM_001166108.2(PALLD):c.2784T>C (p.Pro928=) rs114250766 0.00010
NM_001166108.2(PALLD):c.453C>T (p.Asn151=) rs143682790 0.00009
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.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.3150A>G (p.Val1050=) rs781516286

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