ClinVar Miner

List of variants in gene SMARCA4 studied for Coffin-Siris syndrome 1

Included ClinVar conditions (3):
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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP
NM_001128849.2(SMARCA4):c.*25C>T rs189436737
NM_001128849.2(SMARCA4):c.*299C>T rs772399601
NM_001128849.2(SMARCA4):c.*327T>C rs146968124
NM_001128849.2(SMARCA4):c.*346G>A rs754087248
NM_001128849.2(SMARCA4):c.*401G>A rs559071626
NM_001128849.2(SMARCA4):c.*464G>T rs886054156
NM_001128849.2(SMARCA4):c.-32+11C>T rs886054150
NM_001128849.2(SMARCA4):c.-43C>T rs574982898
NM_001128849.2(SMARCA4):c.-72C>T rs559144002
NM_001128849.2(SMARCA4):c.1076G>A (p.Arg359Gln) rs148530368
NM_001128849.2(SMARCA4):c.1099C>T (p.Leu367=) rs372379166
NM_001128849.2(SMARCA4):c.1104G>A (p.Gln368=) rs751242644
NM_001128849.2(SMARCA4):c.1114T>C (p.Tyr372His) rs140192268
NM_001128849.2(SMARCA4):c.1119-12C>T rs113870824
NM_001128849.2(SMARCA4):c.120C>T (p.His40=) rs375884151
NM_001128849.2(SMARCA4):c.1413G>A (p.Lys471=) rs17001073
NM_001128849.2(SMARCA4):c.1419+7T>C rs112977340
NM_001128849.2(SMARCA4):c.1419+8C>T rs115492175
NM_001128849.2(SMARCA4):c.1419+9C>T rs374635008
NM_001128849.2(SMARCA4):c.147G>A (p.Pro49=) rs758438795
NM_001128849.2(SMARCA4):c.1509A>G (p.Ala503=) rs17001075
NM_001128849.2(SMARCA4):c.1524T>C (p.His508=) rs7935
NM_001128849.2(SMARCA4):c.1557C>T (p.Asn519=) rs2288845
NM_001128849.2(SMARCA4):c.1740A>G (p.Lys580=) rs114391904
NM_001128849.2(SMARCA4):c.1761+6C>T rs886054152
NM_001128849.2(SMARCA4):c.1791T>G (p.Pro597=) rs141806282
NM_001128849.2(SMARCA4):c.1944-12C>T rs149763341
NM_001128849.2(SMARCA4):c.2001+8T>G rs112549813
NM_001128849.2(SMARCA4):c.2085C>T (p.Ser695=) rs149342641
NM_001128849.2(SMARCA4):c.2123+12C>T rs17001090
NM_001128849.2(SMARCA4):c.222+14T>C rs112825147
NM_001128849.2(SMARCA4):c.223-5C>T rs376775933
NM_001128849.2(SMARCA4):c.2232G>C (p.Lys744Asn) rs886054153
NM_001128849.2(SMARCA4):c.2275-3C>A rs117611401
NM_001128849.2(SMARCA4):c.2388C>T (p.Leu796=) rs28997580
NM_001128849.2(SMARCA4):c.2565C>T (p.Val855=) rs775610559
NM_001128849.2(SMARCA4):c.2616+14G>T rs886054154
NM_001128849.2(SMARCA4):c.2757C>T (p.Pro919=) rs113955216
NM_001128849.2(SMARCA4):c.2832C>T (p.Asn944=) rs764939990
NM_001128849.2(SMARCA4):c.2973+14G>A rs372877301
NM_001128849.2(SMARCA4):c.3045C>T (p.Gly1015=) rs56101423
NM_001128849.2(SMARCA4):c.3066C>T (p.Ser1022=) rs149111403
NM_001128849.2(SMARCA4):c.3435C>T (p.Pro1145=) rs138764713
NM_001128849.2(SMARCA4):c.3547-11T>C rs190104006
NM_001128849.2(SMARCA4):c.355+9C>T rs767575401
NM_001128849.2(SMARCA4):c.3558G>A (p.Ala1186=) rs140322802
NM_001128849.2(SMARCA4):c.356-14A>G rs111447132
NM_001128849.2(SMARCA4):c.3669C>T (p.Asn1223=) rs28997581
NM_001128849.2(SMARCA4):c.3738C>T (p.Phe1246=) rs139943231
NM_001128849.2(SMARCA4):c.3775-12A>G rs770956288
NM_001128849.2(SMARCA4):c.3975C>T (p.Arg1325=) rs144803359
NM_001128849.2(SMARCA4):c.4011C>T (p.Leu1337=) rs377720149
NM_001128849.2(SMARCA4):c.4053C>T (p.Asp1351=) rs28997582
NM_001128849.2(SMARCA4):c.4110C>T (p.Gly1370=) rs780735376
NM_001128849.2(SMARCA4):c.4152G>A (p.Thr1384=) rs372620534
NM_001128849.2(SMARCA4):c.4171-9T>A rs201309716
NM_001128849.2(SMARCA4):c.4256G>A (p.Arg1419His) rs775807962
NM_001128849.2(SMARCA4):c.4267-13A>G rs201298366
NM_001128849.2(SMARCA4):c.4328G>A (p.Arg1443Gln) rs886054155
NM_001128849.2(SMARCA4):c.4368G>A (p.Pro1456=) rs114882905
NM_001128849.2(SMARCA4):c.4389C>T (p.Arg1463=) rs149670457
NM_001128849.2(SMARCA4):c.442G>A (p.Gly148Arg) rs138689221
NM_001128849.2(SMARCA4):c.4590C>T (p.Tyr1530=) rs139505007
NM_001128849.2(SMARCA4):c.459G>A (p.Pro153=) rs372931195
NM_001128849.2(SMARCA4):c.4608C>T (p.Pro1536=) rs145435121
NM_001128849.2(SMARCA4):c.4680C>T (p.Asp1560=) rs9105
NM_001128849.2(SMARCA4):c.4731+12G>A rs34930626
NM_001128849.2(SMARCA4):c.4788C>T (p.Ile1596=) rs746415437
NM_001128849.2(SMARCA4):c.4864+15G>C rs113131294
NM_001128849.2(SMARCA4):c.4968G>A (p.Pro1656=) rs182644267
NM_001128849.2(SMARCA4):c.4983T>C (p.Asp1661=) rs7275
NM_001128849.2(SMARCA4):c.5000A>G (p.Gln1667Arg) rs1568566518
NM_001128849.2(SMARCA4):c.584C>A (p.Pro195His) rs1568422604
NM_001128849.2(SMARCA4):c.589C>T (p.Pro197Ser) rs200664441
NM_001128849.2(SMARCA4):c.665C>T (p.Pro222Leu) rs533671711
NM_001128849.2(SMARCA4):c.747C>T (p.Tyr249=) rs756224211
NM_001128849.2(SMARCA4):c.859+7T>A rs141461778
NM_001128849.2(SMARCA4):c.915G>A (p.Pro305=) rs149573400
NM_001128849.2(SMARCA4):c.930C>A (p.Arg310=) rs146141457
NM_001128849.2(SMARCA4):c.968C>T (p.Ser323Leu) rs886054151
NM_001128849.2(SMARCA4):c.981A>C (p.Pro327=) rs547268941

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