ClinVar Miner

List of variants in gene STK11 studied for pancreatic neoplasm

Included ClinVar conditions (36):
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Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.598-8C>T rs373610101 0.00123
NM_000455.5(STK11):c.894C>A (p.Phe298Leu) rs199681533 0.00100
NM_000455.5(STK11):c.1194G>A (p.Ala398=) rs184271025 0.00023
NM_000455.5(STK11):c.464+10C>T rs587782445 0.00003
NM_000455.5(STK11):c.566C>T (p.Thr189Ile) rs587781515 0.00003
NM_000455.5(STK11):c.464+5G>A rs587781681 0.00002
NM_000455.5(STK11):c.1148G>A (p.Arg383His) rs730881990 0.00001
NM_000455.5(STK11):c.1183A>G (p.Thr395Ala) rs587782138 0.00001
NM_000455.5(STK11):c.1195C>A (p.Gln399Lys) rs1060499968 0.00001
NM_000455.5(STK11):c.1208A>G (p.Lys403Arg) rs587781633 0.00001
NM_000455.5(STK11):c.299A>G (p.Gln100Arg) rs1060499957 0.00001
NM_000455.5(STK11):c.358G>A (p.Glu120Lys) rs775595174 0.00001
NM_000455.5(STK11):c.431C>T (p.Pro144Leu) rs1006375117 0.00001
NM_000455.5(STK11):c.434A>G (p.Glu145Gly) rs369764220 0.00001
NM_000455.5(STK11):c.632G>A (p.Arg211Gln) rs730881982 0.00001
NM_000455.5(STK11):c.94A>G (p.Thr32Ala) rs755210880 0.00001
NM_000455.5(STK11):c.108C>A (p.Tyr36Ter) rs137853079
NM_000455.5(STK11):c.1180G>A (p.Gly394Ser) rs768780695
NM_000455.5(STK11):c.1243C>G (p.Arg415Gly) rs864622448
NM_000455.5(STK11):c.124C>T (p.Arg42Trp) rs765367492
NM_000455.5(STK11):c.248A>G (p.Lys83Arg) rs374006397
NM_000455.5(STK11):c.25C>G (p.Leu9Val) rs876661079
NM_000455.5(STK11):c.374T>C (p.Met125Thr)
NM_000455.5(STK11):c.375-19del rs2080764943
NM_000455.5(STK11):c.388dup (p.Glu130fs)
NM_000455.5(STK11):c.486C>T (p.Asp162=) rs1269329328
NM_000455.5(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.5(STK11):c.650del (p.Pro217fs) rs397518442
NM_000455.5(STK11):c.716G>A (p.Trp239Ter) rs730881975
NM_000455.5(STK11):c.719C>G (p.Ser240Trp) rs730881976
NM_000455.5(STK11):c.747C>T (p.Thr249=) rs759546076
NM_000455.5(STK11):c.79C>T (p.His27Tyr)
NM_000455.5(STK11):c.810del (p.Ser271fs)
NM_000455.5(STK11):c.842C>A (p.Pro281Gln) rs121913322
NM_000455.5(STK11):c.936del (p.Lys312fs) rs397518443

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