ClinVar Miner

List of variants in gene STAT3 reported as likely benign for not provided

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_139276.3(STAT3):c.550+210A>C rs35162488 0.20465
NM_139276.3(STAT3):c.550+190C>A rs62075768 0.03709
NM_139276.3(STAT3):c.550+230A>C rs76487950 0.02064
NM_139276.3(STAT3):c.550+250C>A rs868518205 0.01757
NM_139276.3(STAT3):c.273+263G>A rs112232969 0.01443
NM_139276.3(STAT3):c.2144+74T>C rs45540033 0.01386
NM_139276.3(STAT3):c.1888+205A>G rs17879962 0.01383
NM_139276.3(STAT3):c.2102-79G>A rs17885291 0.01319
NM_139276.3(STAT3):c.274-128C>G rs17884756 0.01123
NM_139276.3(STAT3):c.797+156C>A rs17881759 0.00714
NM_139276.3(STAT3):c.128+64T>C rs17882334 0.00702
NM_139276.3(STAT3):c.2257+31A>G rs114401618 0.00559
NM_139276.3(STAT3):c.551-84C>A rs113751085 0.00285
NM_139276.3(STAT3):c.273+22A>G rs2291282 0.00035
NM_139276.3(STAT3):c.2288C>T (p.Ser763Leu) rs140604473 0.00014
NM_139276.3(STAT3):c.1143C>G (p.Ser381=) rs143571879 0.00013
NM_139276.3(STAT3):c.2228G>T (p.Gly743Val) rs151033214 0.00011
NM_139276.3(STAT3):c.405C>T (p.Ala135=) rs201846078 0.00008
NM_139276.3(STAT3):c.2091T>A (p.Ala697=) rs200529713 0.00006
NM_139276.3(STAT3):c.9A>G (p.Gln3=) rs749859511 0.00002
NM_139276.3(STAT3):c.1203C>T (p.Asn401=) rs189708970 0.00001
NM_139276.3(STAT3):c.1601-8_1601-7insG rs1555564070 0.00001
NM_139276.3(STAT3):c.1743C>T (p.Asn581=) rs1141144 0.00001
NM_139276.3(STAT3):c.1233+44G>C
NM_139276.3(STAT3):c.1365+143_1365+146del rs143987966
NM_139276.3(STAT3):c.1365+146dup rs143987966
NM_139276.3(STAT3):c.273+145T>C rs117120730
NM_139276.3(STAT3):c.468+58del rs397712608
NM_139276.3(STAT3):c.551-77ATTCCCTCAGGTCAAGGAGT[2] rs768181932
NM_139276.3(STAT3):c.551-84_551-25del
NM_139276.3(STAT3):c.78C>T (p.Phe26=)
NM_139276.3(STAT3):c.909G>A (p.Pro303=)
STAT3:c.1601-72_1601-71del rs149538586
STAT3:c.469-34_469-30del rs140846959

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