ClinVar Miner

List of variants in gene STAT3 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_139276.3(STAT3):c.1654-11C>G rs17882035 0.00917
NM_139276.3(STAT3):c.1381G>C (p.Val461Leu) rs149214040 0.00612
NM_139276.3(STAT3):c.1680C>T (p.Ser560=) rs146817483 0.00145
NM_139276.3(STAT3):c.551-4G>A rs80162032 0.00115
NM_139276.3(STAT3):c.1329C>T (p.Thr443=) rs147955721 0.00091
NM_139276.3(STAT3):c.2281T>C (p.Leu761=) rs142236792 0.00054
NM_139276.3(STAT3):c.825T>G (p.Leu275=) rs200098006 0.00023
NM_139276.3(STAT3):c.1234-4dup rs763332844 0.00011
NM_139276.3(STAT3):c.2082T>A (p.His694Gln) rs139701269 0.00011
NM_139276.3(STAT3):c.1519G>T (p.Val507Phe) rs145786768 0.00008
NM_139276.3(STAT3):c.2091T>A (p.Ala697=) rs200529713 0.00006
NM_139276.3(STAT3):c.1049+9T>G rs374408588 0.00003
NM_139276.3(STAT3):c.1465-16G>A rs189319171 0.00003
NM_139276.3(STAT3):c.2050G>C (p.Gly684Arg) rs780466766 0.00002
NM_139276.3(STAT3):c.1919A>T (p.Tyr640Phe) rs769031989 0.00001
NM_139276.3(STAT3):c.1981G>T (p.Asp661Tyr) rs747639500 0.00001
NM_139276.3(STAT3):c.368C>T (p.Ala123Val) rs1475754644 0.00001
NM_139276.3(STAT3):c.372+10G>C rs766222549 0.00001
NM_139276.3(STAT3):c.*123dup
NM_139276.3(STAT3):c.1003C>T (p.Arg335Trp) rs193922716
NM_139276.3(STAT3):c.1145G>A (p.Arg382Gln) rs113994136
NM_139276.3(STAT3):c.1229A>G (p.His410Arg) rs2144772044
NM_139276.3(STAT3):c.1234A>T (p.Thr412Ser) rs1567713850
NM_139276.3(STAT3):c.1243G>A (p.Glu415Lys) rs193922717
NM_139276.3(STAT3):c.1365+143_1365+146del rs143987966
NM_139276.3(STAT3):c.1365+146dup rs143987966
NM_139276.3(STAT3):c.1366-20A>G rs1567710255
NM_139276.3(STAT3):c.1384GTG[1] (p.Val463del) rs113994138
NM_139276.3(STAT3):c.1397A>G (p.Asn466Ser) rs1057521091
NM_139276.3(STAT3):c.1772A>T (p.Lys591Met) rs193922719
NM_139276.3(STAT3):c.1780G>A (p.Glu594Lys) rs193922720
NM_139276.3(STAT3):c.1840A>C (p.Ser614Arg) rs886039546
NM_139276.3(STAT3):c.1849G>A (p.Gly617Arg) rs2144691698
NM_139276.3(STAT3):c.1852G>C (p.Gly618Arg) rs2081548277
NM_139276.3(STAT3):c.1863C>G (p.Phe621Leu) rs1555563854
NM_139276.3(STAT3):c.1909G>A (p.Val637Met) rs113994139
NM_139276.3(STAT3):c.1919_1920delinsTT (p.Tyr640Phe) rs2081522163
NM_139276.3(STAT3):c.1940A>T (p.Asn647Ile) rs770986654
NM_139276.3(STAT3):c.1940_1941delinsTT (p.Asn647Ile)
NM_139276.3(STAT3):c.1970A>G (p.Tyr657Cys) rs193922721
NM_139276.3(STAT3):c.1979T>C (p.Met660Thr) rs886039434
NM_139276.3(STAT3):c.2134T>C (p.Cys712Arg) rs193922722
NM_139276.3(STAT3):c.2144+46_2144+47del rs1279773038
NM_139276.3(STAT3):c.2144+9C>G
NM_139276.3(STAT3):c.432G>A (p.Leu144=)
NM_139276.3(STAT3):c.921G>A (p.Glu307=)
STAT3:c.1601-72_1601-71del rs149538586
STAT3:c.469-34_469-30del rs140846959

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