ClinVar Miner

List of variants in gene GATA3 studied for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
GATA3, 1-BP DEL, 431G
GATA3, 1-BP DEL, 478G
GATA3, 12-BP DEL, NT946-957
GATA3, 2-BP DEL, 108GG
GATA3, 2-BP INS, 3-BP INS
GATA3, 250-KB DEL
GATA3, 49-BP DEL, NT465-513
GATA3, 900-KB DEL
NM_001002295.1(GATA3):c.-370+28delT rs397846644
NM_001002295.1(GATA3):c.-370+28dupT rs397846644
NM_001002295.2(GATA3):c.*1029C>T rs530772797
NM_001002295.2(GATA3):c.*105A>G rs886047300
NM_001002295.2(GATA3):c.*1066C>T rs11255509
NM_001002295.2(GATA3):c.*1072C>A rs886047306
NM_001002295.2(GATA3):c.*264_*265dup rs3839918
NM_001002295.2(GATA3):c.*265dup rs3839918
NM_001002295.2(GATA3):c.*267G>A rs886047301
NM_001002295.2(GATA3):c.*26C>G rs200946839
NM_001002295.2(GATA3):c.*356G>A rs886047302
NM_001002295.2(GATA3):c.*491A>G rs138815232
NM_001002295.2(GATA3):c.*517A>G rs9746
NM_001002295.2(GATA3):c.*575A>C rs552915242
NM_001002295.2(GATA3):c.*612G>A rs1058240
NM_001002295.2(GATA3):c.*647A>G rs563624409
NM_001002295.2(GATA3):c.*664C>T rs192494656
NM_001002295.2(GATA3):c.*714G>A rs886047303
NM_001002295.2(GATA3):c.*746C>T rs545858251
NM_001002295.2(GATA3):c.*798G>A rs531077807
NM_001002295.2(GATA3):c.*857A>T rs886047304
NM_001002295.2(GATA3):c.*895T>G rs886047305
NM_001002295.2(GATA3):c.*93C>T rs2229360
NM_001002295.2(GATA3):c.*952G>A rs773450577
NM_001002295.2(GATA3):c.-148A>G rs886047299
NM_001002295.2(GATA3):c.-251G>A rs10905277
NM_001002295.2(GATA3):c.-264G>T rs35971003
NM_001002295.2(GATA3):c.-287G>A rs886047298
NM_001002295.2(GATA3):c.-351C>T rs34628951
NM_001002295.2(GATA3):c.-359G>A rs138512915
NM_001002295.2(GATA3):c.-369-11C>T rs886047297
NM_001002295.2(GATA3):c.-413C>T rs540527013
NM_001002295.2(GATA3):c.-48G>T rs554517990
NM_001002295.2(GATA3):c.-49C>T rs11567942
NM_001002295.2(GATA3):c.-503_-502dup rs60098638
NM_001002295.2(GATA3):c.-58C>T rs412359
NM_001002295.2(GATA3):c.-60C>T rs11567887
NM_001002295.2(GATA3):c.-69G>A rs28395794
NM_001002295.2(GATA3):c.-95G>T rs369825935
NM_001002295.2(GATA3):c.1025G>A (p.Cys342Tyr) rs387906621
NM_001002295.2(GATA3):c.1058G>C (p.Arg353Thr) rs1564405163
NM_001002295.2(GATA3):c.1059A>T (p.Arg353Ser) rs104894165
NM_001002295.2(GATA3):c.1099C>T (p.Arg367Ter) rs104894164
NM_001002295.2(GATA3):c.1179C>T (p.Asn393=) rs138679257
NM_001002295.2(GATA3):c.1223C>T (p.Ser408Leu) rs752977342
NM_001002295.2(GATA3):c.1257G>A (p.Thr419=) rs11567941
NM_001002295.2(GATA3):c.1266G>A (p.Pro422=) rs541782074
NM_001002295.2(GATA3):c.216G>T (p.Val72=) rs560531559
NM_001002295.2(GATA3):c.436G>A (p.Ala146Thr) rs752779081
NM_001002295.2(GATA3):c.480C>G (p.Asp160Glu) rs143627754
NM_001002295.2(GATA3):c.573C>T (p.Pro191=) rs35508267
NM_001002295.2(GATA3):c.57C>T (p.Leu19=) rs749900784
NM_001002295.2(GATA3):c.606T>C (p.Arg202=) rs2228254
NM_001002295.2(GATA3):c.621C>T (p.Ala207=) rs2229359
NM_001002295.2(GATA3):c.631G>A (p.Ala211Thr) rs778421571
NM_001002295.2(GATA3):c.681_682insACCACCCCATCAGCACTCACCCGCCCTACGTGCCC (p.Glu228fs) rs878853222
NM_001002295.2(GATA3):c.706C>G (p.Pro236Ala) rs148835259
NM_001002295.2(GATA3):c.72G>A (p.Pro24=) rs202168967
NM_001002295.2(GATA3):c.823T>A (p.Trp275Arg) rs104894163
NM_001002295.2(GATA3):c.829C>T (p.Arg277Ter) rs104894162
NM_001002295.2(GATA3):c.840G>C (p.Thr280=) rs144796042
NM_001002295.2(GATA3):c.870C>T (p.Leu290=) rs575091
NM_001002295.2(GATA3):c.924+2delinsGCTTACTTCCC rs387906551

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