ClinVar Miner

List of variants reported as benign for Pancreatic cancer, susceptibility to, 1 by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001166108.2(PALLD):c.1965-12625A>G rs62333013 0.49745
NM_001166108.2(PALLD):c.678C>T (p.Asp226=) rs7673220 0.29605
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.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.1965-12953C>T rs528879194 0.00493
NM_001166108.2(PALLD):c.2442A>G (p.Thr814=) rs113676921 0.00218
NM_001166108.2(PALLD):c.3256C>T (p.Leu1086=) rs59633770 0.00098
NM_001166108.2(PALLD):c.2199+8G>A rs200060953 0.00070
NM_001166108.2(PALLD):c.1965-12530C>T rs753092219 0.00009
NM_001166108.2(PALLD):c.1965-12565G>A rs368350042 0.00004

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