ClinVar Miner

List of variants in gene STAT3 studied for not specified

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_139276.3(STAT3):c.1233+43C>G rs2293152 0.66160
NM_139276.3(STAT3):c.1888+142C>G rs8081431 0.18660
NM_139276.3(STAT3):c.2144+20C>T rs8069115 0.03624
NM_139276.3(STAT3):c.1381G>C (p.Val461Leu) rs149214040 0.00612
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.1854C>T (p.Gly618=) rs117691970 0.00089
NM_139276.3(STAT3):c.225G>A (p.Ser75=) rs146184566 0.00089
NM_139276.3(STAT3):c.1492A>G (p.Ile498Val) rs146620441 0.00078
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.2288C>T (p.Ser763Leu) rs140604473 0.00014
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.373-4G>C rs376611360 0.00010
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.1366-9C>T rs375054973 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.1366-11T>C rs761523186 0.00001
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.373C>G (p.Gln125Glu) rs574370336 0.00001
NM_139276.3(STAT3):c.*123dup
NM_139276.3(STAT3):c.1229A>G (p.His410Arg) rs2144772044
NM_139276.3(STAT3):c.1233+20C>T rs761232183
NM_139276.3(STAT3):c.1250G>C (p.Arg417Thr)
NM_139276.3(STAT3):c.1281+11T>C rs776564054
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.1600+11C>T rs1204881810
NM_139276.3(STAT3):c.1601-10dup rs3830585
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.1888+6G>A rs1555563842
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.2144+46_2144+47del rs1279773038
NM_139276.3(STAT3):c.2144+9C>G
NM_139276.3(STAT3):c.468+58del rs397712608
NM_139276.3(STAT3):c.484A>G (p.Met162Val)
NM_139276.3(STAT3):c.551-57_551-18del rs768181932
STAT3:c.469-34_469-30del rs140846959

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