ClinVar Miner

List of variants in gene PALLD studied for Pancreatic cancer, susceptibility to, 1

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Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.1965-12625A>G rs62333013 0.49745
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.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.1965-12953C>T rs528879194 0.00493
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.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.1849C>T (p.Arg617Cys) rs138283237 0.00102
NM_001166108.2(PALLD):c.1965-12594T>G rs587780760 0.00102
NM_001166108.2(PALLD):c.-179G>C rs540595354 0.00088
NM_001166108.2(PALLD):c.539C>T (p.Thr180Ile) rs146387060 0.00071
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.-83+9G>A rs150719521 0.00037
NM_001166108.2(PALLD):c.8G>T (p.Gly3Val) rs189385916 0.00036
NM_001166108.2(PALLD):c.1965-12616C>T rs121908291 0.00026
NM_001166108.2(PALLD):c.-143A>G rs571957605 0.00024
NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln) rs145571230 0.00016
NM_001166108.2(PALLD):c.1842T>A (p.His614Gln) rs150443035 0.00016
NM_001166108.2(PALLD):c.1386C>T (p.Cys462=) rs199755853 0.00014
NM_001166108.2(PALLD):c.-115C>G rs189011214 0.00011
NM_001166108.2(PALLD):c.195G>A (p.Ser65=) rs369178136 0.00011
NM_001166108.2(PALLD):c.-135A>G rs540285834 0.00009
NM_001166108.2(PALLD):c.1965-12530C>T rs753092219 0.00009
NM_001166108.2(PALLD):c.453C>T (p.Asn151=) rs143682790 0.00009
NM_001166108.2(PALLD):c.413G>A (p.Arg138Gln) rs138665337 0.00007
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.428G>A (p.Arg143His) rs149345491 0.00006
NM_001166108.2(PALLD):c.229G>C (p.Glu77Gln) rs376732578 0.00005
NM_001166108.2(PALLD):c.366T>G (p.Pro122=) rs377747204 0.00005
NM_001166108.2(PALLD):c.1433G>A (p.Gly478Glu) rs201816881 0.00004
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.1965-12800C>T rs863224383 0.00002
NM_001166108.2(PALLD):c.860G>A (p.Arg287Gln) rs141283998 0.00002
NM_001166108.2(PALLD):c.-172C>A rs777479051 0.00001
NM_001166108.2(PALLD):c.-178G>A rs886059207 0.00001
NM_001166108.2(PALLD):c.107A>G (p.Gln36Arg) rs889514388 0.00001
NM_001166108.2(PALLD):c.1129A>G (p.Lys377Glu) rs368684220 0.00001
NM_001166108.2(PALLD):c.1219A>T (p.Thr407Ser) rs775730191 0.00001
NM_001166108.2(PALLD):c.1260+8T>C rs887513464 0.00001
NM_001166108.2(PALLD):c.222C>T (p.Ser74=) rs201038000 0.00001
NM_001166108.2(PALLD):c.472C>A (p.His158Asn) rs777197884 0.00001
NM_001166108.2(PALLD):c.608G>T (p.Gly203Val) rs770458533 0.00001
NM_001166108.2(PALLD):c.65A>G (p.Lys22Arg) rs201343910 0.00001
NM_001166108.2(PALLD):c.836G>C (p.Ser279Thr) rs886059209 0.00001
NM_001166108.2(PALLD):c.-162C>T rs538959058
NM_001166108.2(PALLD):c.1011C>A (p.Asp337Glu) rs763283965
NM_001166108.2(PALLD):c.1571G>T (p.Arg524Ile) rs776908136
NM_001166108.2(PALLD):c.1616C>T (p.Thr539Ile) rs780510622
NM_001166108.2(PALLD):c.1926C>G (p.Pro642=) rs886059210
NM_001166108.2(PALLD):c.1957C>A (p.Pro653Thr) rs1784873065
NM_001166108.2(PALLD):c.296C>A (p.Ser99Ter)
NM_001166108.2(PALLD):c.353C>G (p.Ser118Ter)
NM_001166108.2(PALLD):c.574A>G (p.Ser192Gly) rs1762575507
NM_001166108.2(PALLD):c.622A>G (p.Lys208Glu)
NM_001166108.2(PALLD):c.639C>A (p.Ala213=) rs1762581096
NM_001166108.2(PALLD):c.721C>T (p.His241Tyr) rs1490249027
NM_001166108.2(PALLD):c.908+3A>G rs1762604026
NM_001166108.2(PALLD):c.946G>T (p.Asp316Tyr) rs1477916241

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