ClinVar Miner

List of variants in gene STK11 reported as likely benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.426C>T (p.Ser142=) rs758448869 0.00053
NM_000455.5(STK11):c.366G>A (p.Lys122=) rs376969448 0.00005
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.678C>T (p.Asn226=) rs748832988 0.00005
NM_000455.5(STK11):c.566C>T (p.Thr189Ile) rs587781515 0.00003
NM_000455.5(STK11):c.588C>T (p.Gly196=) rs769309428 0.00003
NM_000455.5(STK11):c.615G>A (p.Ala205=) rs532889728 0.00003
NM_000455.5(STK11):c.876C>T (p.Tyr292=) rs148928808 0.00003
NM_000455.5(STK11):c.597+9G>A rs863224361 0.00002
NM_000455.5(STK11):c.1128G>A (p.Glu376=) rs747018506 0.00001
NM_000455.5(STK11):c.1190C>T (p.Ala397Val) rs558040549 0.00001
NM_000455.5(STK11):c.1278G>A (p.Arg426=) rs201256614 0.00001
NM_000455.5(STK11):c.15C>T (p.Asp5=) rs786201498 0.00001
NM_000455.5(STK11):c.279C>G (p.Ala93=) rs786201852 0.00001
NM_000455.5(STK11):c.396C>T (p.Cys132=) rs730881969 0.00001
NM_000455.5(STK11):c.441T>C (p.Arg147=) rs786201456 0.00001
NM_000455.5(STK11):c.559G>A (p.Gly187Ser) rs587782032 0.00001
NM_000455.5(STK11):c.594C>T (p.Ala198=) rs772940660 0.00001
NM_000455.5(STK11):c.632G>A (p.Arg211Gln) rs730881982 0.00001
NM_000455.5(STK11):c.720G>A (p.Ser240=) rs759743897 0.00001
NM_000455.5(STK11):c.765C>T (p.Phe255=) rs769912677 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NM_000455.5(STK11):c.957A>G (p.Pro319=) rs755126393 0.00001
NM_000455.5(STK11):c.117C>T (p.Arg39=) rs786203942
NM_000455.5(STK11):c.1191G>A (p.Ala397=) rs774759899
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.5(STK11):c.1284G>T (p.Ser428=) rs369097329
NM_000455.5(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.5(STK11):c.435G>A (p.Glu145=) rs1555737810
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.490C>T (p.Leu164=)
NM_000455.5(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.5(STK11):c.609G>C (p.Pro203=) rs786201228
NM_000455.5(STK11):c.735-10C>T rs553975112
NM_000455.5(STK11):c.756G>A (p.Leu252=) rs786201544
NM_000455.5(STK11):c.90C>T (p.Asp30=) rs771765869
NM_000455.5(STK11):c.920+7G>T rs2075607

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