ClinVar Miner

List of variants in gene STK11 reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Total variants: 36
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HGVS dbSNP
NM_000455.4(STK11):c.-1C>T rs759284466
NM_000455.4(STK11):c.1015C>G (p.Pro339Ala) rs769644352
NM_000455.4(STK11):c.1027G>A (p.Asp343Asn) rs368547224
NM_000455.4(STK11):c.1038C>T (p.Gly346=) rs767565606
NM_000455.4(STK11):c.1044C>T (p.Asp348=) rs778274196
NM_000455.4(STK11):c.1063G>A (p.Asp355Asn) rs769403473
NM_000455.4(STK11):c.1069G>A (p.Glu357Lys) rs759473833
NM_000455.4(STK11):c.1108+3G>A rs755746417
NM_000455.4(STK11):c.1109-4C>T rs1407794756
NM_000455.4(STK11):c.1127A>C (p.Glu376Ala) rs373888280
NM_000455.4(STK11):c.1142G>C (p.Gly381Ala) rs765419233
NM_000455.4(STK11):c.1163A>G (p.Lys388Arg) rs756877141
NM_000455.4(STK11):c.116G>T (p.Arg39Leu) rs786203250
NM_000455.4(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.4(STK11):c.1248G>C (p.Lys416Asn) rs1459406168
NM_000455.4(STK11):c.1254C>G (p.Cys418Trp) rs587780715
NM_000455.4(STK11):c.15C>T (p.Asp5=) rs786201498
NM_000455.4(STK11):c.298C>G (p.Gln100Glu) rs757841535
NM_000455.4(STK11):c.301C>G (p.Leu101Val) rs587780716
NM_000455.4(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.4(STK11):c.396C>T (p.Cys132=) rs730881969
NM_000455.4(STK11):c.397G>A (p.Val133Met) rs567769257
NM_000455.4(STK11):c.425G>A (p.Ser142Asn) rs1568705518
NM_000455.4(STK11):c.434A>G (p.Glu145Gly) rs369764220
NM_000455.4(STK11):c.435G>A (p.Glu145=) rs1555737810
NM_000455.4(STK11):c.441T>C (p.Arg147=) rs786201456
NM_000455.4(STK11):c.465-5C>A rs567202367
NM_000455.4(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.4(STK11):c.559G>A (p.Gly187Ser) rs587782032
NM_000455.4(STK11):c.566C>T (p.Thr189Ile) rs587781515
NM_000455.4(STK11):c.817G>A (p.Ala273Thr) rs587782199
NM_000455.4(STK11):c.876C>T (p.Tyr292=) rs148928808
NM_000455.4(STK11):c.90C>T (p.Asp30=) rs771765869
NM_000455.4(STK11):c.920+5G>A rs587780013
NM_000455.4(STK11):c.920+7G>A rs2075607
NM_000455.4(STK11):c.920+7G>T rs2075607

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