ClinVar Miner

List of variants in gene KCNJ10 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (916):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_002241.5(KCNJ10):c.1015C>A (p.Pro339Thr) rs1557967589
NM_002241.5(KCNJ10):c.1015C>T (p.Pro339Ser) rs1557967589
NM_002241.5(KCNJ10):c.1042C>T (p.Arg348Cys) rs137853074
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His) rs146396982
NM_002241.5(KCNJ10):c.1048G>A (p.Gly350Arg) rs770453248
NM_002241.5(KCNJ10):c.1051G>A (p.Asp351Asn) rs373899425
NM_002241.5(KCNJ10):c.1054C>A (p.Pro352Thr)
NM_002241.5(KCNJ10):c.1061A>G (p.Lys354Arg) rs142596580
NM_002241.5(KCNJ10):c.106C>T (p.Arg36Cys)
NM_002241.5(KCNJ10):c.1102G>C (p.Glu368Gln) rs377330985
NM_002241.5(KCNJ10):c.1123C>T (p.Arg375Cys) rs751338154
NM_002241.5(KCNJ10):c.1124G>A (p.Arg375His) rs189596680
NM_002241.5(KCNJ10):c.133G>A (p.Ala45Thr) rs750246232
NM_002241.5(KCNJ10):c.143G>C (p.Arg48Pro)
NM_002241.5(KCNJ10):c.148C>T (p.Leu50Phe) rs773510302
NM_002241.5(KCNJ10):c.179T>C (p.Ile60Thr) rs759993423
NM_002241.5(KCNJ10):c.221C>T (p.Thr74Ile) rs796052604
NM_002241.5(KCNJ10):c.250G>A (p.Val84Met) rs140646329
NM_002241.5(KCNJ10):c.264G>A (p.Leu88=)
NM_002241.5(KCNJ10):c.290T>A (p.Leu97Gln) rs1401791648
NM_002241.5(KCNJ10):c.300C>A (p.Asp100Glu) rs139069413
NM_002241.5(KCNJ10):c.301C>A (p.Pro101Thr) rs375361490
NM_002241.5(KCNJ10):c.305C>T (p.Pro102Leu) rs372156619
NM_002241.5(KCNJ10):c.385A>G (p.Ile129Val)
NM_002241.5(KCNJ10):c.401G>A (p.Arg134His) rs368857205
NM_002241.5(KCNJ10):c.511C>T (p.Arg171Trp) rs769666695
NM_002241.5(KCNJ10):c.512G>A (p.Arg171Gln)
NM_002241.5(KCNJ10):c.524G>A (p.Arg175Gln) rs397514673
NM_002241.5(KCNJ10):c.52C>T (p.Arg18Trp) rs138457635
NM_002241.5(KCNJ10):c.530A>G (p.Glu177Gly) rs145947380
NM_002241.5(KCNJ10):c.62T>C (p.Met21Thr) rs878854483
NM_002241.5(KCNJ10):c.652C>T (p.Leu218Phe) rs558502886
NM_002241.5(KCNJ10):c.688C>T (p.Arg230Trp) rs149615470
NM_002241.5(KCNJ10):c.689G>A (p.Arg230Gln) rs200807361
NM_002241.5(KCNJ10):c.783G>C (p.Glu261Asp)
NM_002241.5(KCNJ10):c.934_935delinsTT (p.Thr312Leu)
NM_002241.5(KCNJ10):c.998T>C (p.Val333Ala) rs750091894

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