ClinVar Miner

List of variants in gene PALLD reported as benign for exocrine pancreatic carcinoma

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
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_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.1965-12665G>C rs535155432 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.1040C>T (p.Thr347Met) rs150711066 0.00065
NM_001166108.2(PALLD):c.365C>T (p.Pro122Leu) rs116158771 0.00064
NM_001166108.2(PALLD):c.1965-12910C>G rs550499593 0.00046
NM_001166108.2(PALLD):c.8G>T (p.Gly3Val) rs189385916 0.00036
NM_001166108.2(PALLD):c.1965-10T>A rs149239490 0.00022
NM_001166108.2(PALLD):c.1289G>A (p.Arg430Gln) rs145571230 0.00016
NM_001166108.2(PALLD):c.1965-13016C>T rs561750970 0.00013
NM_001166108.2(PALLD):c.195G>A (p.Ser65=) rs369178136 0.00011
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.-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.65A>G (p.Lys22Arg) rs201343910 0.00001
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.671_672inv (p.Met224Thr) rs373066707

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