ClinVar Miner

List of variants in gene STK11 studied for carcinoma

Included ClinVar conditions (243):
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Gene type:
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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.375-49G>A rs34928889 0.45190
NM_000455.5(STK11):c.465-51T>C rs2075606 0.29935
NM_000455.5(STK11):c.374+24G>T rs2075604 0.18985
NM_000455.5(STK11):c.264C>A (p.Ile88=) rs56354945 0.02303
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.598-7G>A rs377502057 0.00008
NM_000455.5(STK11):c.465-5C>T rs567202367 0.00005
NM_000455.5(STK11):c.368A>G (p.Gln123Arg) rs764449808 0.00004
NM_000455.5(STK11):c.1193C>T (p.Ala398Val) rs768058962 0.00003
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.358G>A (p.Glu120Lys) rs775595174 0.00001
NM_000455.5(STK11):c.480G>T (p.Leu160=) rs1176365465 0.00001
NM_000455.5(STK11):c.632G>A (p.Arg211Gln) rs730881982 0.00001
NM_000455.5(STK11):c.108C>A (p.Tyr36Ter) rs137853079
NM_000455.5(STK11):c.1109-955A>G
NM_000455.5(STK11):c.1180G>A (p.Gly394Ser) rs768780695
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.5(STK11):c.1243C>G (p.Arg415Gly) rs864622448
NM_000455.5(STK11):c.256C>G (p.Arg86Gly) rs1057520039
NM_000455.5(STK11):c.25C>G (p.Leu9Val) rs876661079
NM_000455.5(STK11):c.375-19del rs2080764943
NM_000455.5(STK11):c.397G>A (p.Val133Met) rs567769257
NM_000455.5(STK11):c.464+44dup rs544282452
NM_000455.5(STK11):c.464+95T>C rs2080767432
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.486C>T (p.Asp162=) rs1269329328
NM_000455.5(STK11):c.487G>T (p.Gly163Cys) rs730881972
NM_000455.5(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.5(STK11):c.580G>A (p.Asp194Asn) rs121913315
NM_000455.5(STK11):c.587G>T (p.Gly196Val) rs1057519858
NM_000455.5(STK11):c.598-32C>T rs2080775539
NM_000455.5(STK11):c.647C>T (p.Ser216Phe) rs1057520017
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.734+14C>A rs763346212
NM_000455.5(STK11):c.747C>T (p.Thr249=) rs759546076
NM_000455.5(STK11):c.842C>A (p.Pro281Gln) rs121913322
NM_000455.5(STK11):c.936del (p.Lys312fs) rs397518443
t(17;19)(q25.1;p13.3)

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