ClinVar Miner

List of variants in gene SETX reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NM_015046.7(SETX):c.*168C>T
NM_015046.7(SETX):c.*2232T>C rs545456048
NM_015046.7(SETX):c.*2506T>C rs73545065
NM_015046.7(SETX):c.*266A>G rs575959163
NM_015046.7(SETX):c.*319C>T rs1056912
NM_015046.7(SETX):c.*431_*432del rs112251805
NM_015046.7(SETX):c.*905A>G rs58327306
NM_015046.7(SETX):c.1221A>G (p.Thr407=) rs377618570
NM_015046.7(SETX):c.1693T>C (p.Phe565Leu) rs143982186
NM_015046.7(SETX):c.1880T>C (p.Met627Thr) rs199707503
NM_015046.7(SETX):c.192A>G (p.Leu64=) rs117326462
NM_015046.7(SETX):c.2216G>A (p.Gly739Glu) rs36024203
NM_015046.7(SETX):c.2672T>C (p.Val891Ala) rs148181729
NM_015046.7(SETX):c.2934C>T (p.Ser978=)
NM_015046.7(SETX):c.3103A>G (p.Lys1035Glu) rs117229601
NM_015046.7(SETX):c.3229G>A (p.Asp1077Asn) rs145097270
NM_015046.7(SETX):c.3310C>G (p.Gln1104Glu) rs113831637
NM_015046.7(SETX):c.3809C>T (p.Pro1270Leu) rs144334281
NM_015046.7(SETX):c.3826C>G (p.Gln1276Glu) rs148604312
NM_015046.7(SETX):c.3992C>T (p.Pro1331Leu) rs11243731
NM_015046.7(SETX):c.4020G>T (p.Lys1340Asn) rs368323660
NM_015046.7(SETX):c.4096T>C (p.Ser1366Pro) rs140147684
NM_015046.7(SETX):c.4197A>G (p.Thr1399=) rs148078248
NM_015046.7(SETX):c.4204A>T (p.Thr1402Ser) rs150421712
NM_015046.7(SETX):c.431A>G (p.Asn144Ser) rs767453182
NM_015046.7(SETX):c.4511A>G (p.Glu1504Gly)
NM_015046.7(SETX):c.4660T>G (p.Cys1554Gly) rs112089123
NM_015046.7(SETX):c.472T>G (p.Leu158Val) rs145438764
NM_015046.7(SETX):c.4989T>A (p.Ser1663=)
NM_015046.7(SETX):c.5271A>G (p.Glu1757=)
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.5786C>T (p.Ala1929Val)
NM_015046.7(SETX):c.5949+5G>A rs374656811
NM_015046.7(SETX):c.60C>T (p.Arg20=) rs553346505
NM_015046.7(SETX):c.6161G>A (p.Ser2054Asn)
NM_015046.7(SETX):c.6435C>T (p.Ile2145=)
NM_015046.7(SETX):c.654G>C (p.Lys218Asn) rs117861188
NM_015046.7(SETX):c.6675C>T (p.Tyr2225=) rs200382898
NM_015046.7(SETX):c.710A>G (p.Tyr237Cys) rs138538492
NM_015046.7(SETX):c.7640T>C (p.Ile2547Thr) rs151117904
NM_015046.7(SETX):c.7724C>T (p.Pro2575Leu) rs34000644
NM_015046.7(SETX):c.7787C>T (p.Ala2596Val) rs200507089
NM_015046.7(SETX):c.7814G>A (p.Arg2605Gln) rs543247171
NM_015046.7(SETX):c.7851G>A (p.Thr2617=)
NM_015046.7(SETX):c.7874C>T (p.Pro2625Leu) rs553413088

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