ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_015046.7(SETX):c.1343A>G (p.Asp448Gly) rs370363342
NM_015046.7(SETX):c.1467C>T (p.Val489=) rs142093830
NM_015046.7(SETX):c.1815T>C (p.Phe605=) rs753675238
NM_015046.7(SETX):c.2216G>A (p.Gly739Glu) rs36024203
NM_015046.7(SETX):c.2479A>G (p.Lys827Glu) rs150532677
NM_015046.7(SETX):c.2490A>C (p.Gly830=) rs751429987
NM_015046.7(SETX):c.2502A>G (p.Gly834=) rs762818441
NM_015046.7(SETX):c.2955G>A (p.Ser985=) rs201251074
NM_015046.7(SETX):c.3018A>C (p.Gly1006=) rs997364371
NM_015046.7(SETX):c.3057_3059TGA[7] (p.Asp1024dup) rs572772837
NM_015046.7(SETX):c.3090T>C (p.Leu1030=) rs368677513
NM_015046.7(SETX):c.3210T>C (p.Leu1070=) rs145014082
NM_015046.7(SETX):c.3229G>A (p.Asp1077Asn) rs145097270
NM_015046.7(SETX):c.3345C>G (p.Ala1115=) rs142020270
NM_015046.7(SETX):c.3450A>G (p.Glu1150=) rs771495291
NM_015046.7(SETX):c.3525G>A (p.Arg1175=) rs1353053473
NM_015046.7(SETX):c.3603T>C (p.Ile1201=) rs565774066
NM_015046.7(SETX):c.3651G>C (p.Thr1217=) rs111419285
NM_015046.7(SETX):c.3813A>G (p.Pro1271=) rs759945253
NM_015046.7(SETX):c.3966C>A (p.Thr1322=) rs772257618
NM_015046.7(SETX):c.399T>C (p.Cys133=) rs779515782
NM_015046.7(SETX):c.4020_4022del (p.Lys1341del) rs769558791
NM_015046.7(SETX):c.4209G>A (p.Glu1403=) rs1347401564
NM_015046.7(SETX):c.4225A>T (p.Asn1409Tyr) rs373375060
NM_015046.7(SETX):c.4273A>G (p.Lys1425Glu) rs534886444
NM_015046.7(SETX):c.4662T>C (p.Cys1554=) rs1589736164
NM_015046.7(SETX):c.4677A>G (p.Lys1559=) rs200123129
NM_015046.7(SETX):c.4872A>G (p.Leu1624=) rs567475841
NM_015046.7(SETX):c.4982C>G (p.Pro1661Arg) rs146873848
NM_015046.7(SETX):c.499-9T>C rs760214195
NM_015046.7(SETX):c.5130T>C (p.Tyr1710=) rs768582274
NM_015046.7(SETX):c.5274+8T>C rs369501754
NM_015046.7(SETX):c.5283A>G (p.Gln1761=) rs139063885
NM_015046.7(SETX):c.5473A>G (p.Thr1825Ala) rs151046729
NM_015046.7(SETX):c.5616C>T (p.Asn1872=) rs201472554
NM_015046.7(SETX):c.5712A>G (p.Arg1904=) rs750372437
NM_015046.7(SETX):c.5782-6A>G rs781129157
NM_015046.7(SETX):c.5814A>G (p.Gln1938=) rs143868969
NM_015046.7(SETX):c.5901A>G (p.Thr1967=) rs780717865
NM_015046.7(SETX):c.5949+5G>A rs374656811
NM_015046.7(SETX):c.6122T>C (p.Ile2041Thr) rs140676924
NM_015046.7(SETX):c.6351C>T (p.Ser2117=) rs200269892
NM_015046.7(SETX):c.6474T>C (p.Ser2158=) rs1216377543
NM_015046.7(SETX):c.6762C>T (p.Leu2254=) rs1225106822
NM_015046.7(SETX):c.7164G>C (p.Thr2388=) rs368602563
NM_015046.7(SETX):c.7287+9C>A rs769170686
NM_015046.7(SETX):c.75T>G (p.Thr25=) rs1589791526
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr) rs151117904
NM_015046.7(SETX):c.7737C>T (p.Val2579=) rs780854409
NM_015046.7(SETX):c.7770C>T (p.Pro2590=) rs532828022
NM_015046.7(SETX):c.7875G>A (p.Pro2625=) rs536241867
NM_015046.7(SETX):c.7926G>A (p.Glu2642=) rs147986724
NM_015046.7(SETX):c.7941T>C (p.Gly2647=) rs1471003365
NM_015046.7(SETX):c.7991T>C (p.Leu2664Pro) rs143798689

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