ClinVar Miner

List of variants reported as likely pathogenic for Pancreatic Neoplasms

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Total variants: 5
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HGVS dbSNP
NM_000455.4(STK11):c.582C>A (p.Asp194Glu) rs786202134
NM_000455.4(STK11):c.582C>G (p.Asp194Glu) rs786202134
NM_003318.5(TTK):c.2089G>T (p.Asp697Tyr) rs1057520011
NM_030906.4(STK33):c.969T>G (p.Phe323Leu) rs1057520013
NM_178170.3(NEK8):c.589G>C (p.Ala197Pro) rs756231248

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