ClinVar Miner

List of variants in gene SPTAN1 reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 130
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HGVS dbSNP
NC_000009.12:g.128586034_128586036del
NM_001130438.3(SPTAN1):c.1092A>G (p.Gln364=) rs570171059
NM_001130438.3(SPTAN1):c.1221+11C>T rs113357847
NM_001130438.3(SPTAN1):c.1221+286T>A
NM_001130438.3(SPTAN1):c.1221+321T>C
NM_001130438.3(SPTAN1):c.1222-226C>G
NM_001130438.3(SPTAN1):c.1222-247G>A
NM_001130438.3(SPTAN1):c.1222-274T>C
NM_001130438.3(SPTAN1):c.1330G>A (p.Val444Ile) rs77358650
NM_001130438.3(SPTAN1):c.1461+14A>C rs376751145
NM_001130438.3(SPTAN1):c.1462-27T>A rs7040737
NM_001130438.3(SPTAN1):c.1511C>T (p.Ala504Val) rs148727077
NM_001130438.3(SPTAN1):c.1710C>T (p.Ala570=) rs115428827
NM_001130438.3(SPTAN1):c.1737C>T (p.Phe579=) rs143941068
NM_001130438.3(SPTAN1):c.1807-11T>C rs139049596
NM_001130438.3(SPTAN1):c.2011+10G>A rs377437879
NM_001130438.3(SPTAN1):c.2011+28A>G
NM_001130438.3(SPTAN1):c.2012-146T>C
NM_001130438.3(SPTAN1):c.2163= (p.Ala721=) rs10760566
NM_001130438.3(SPTAN1):c.2194-13T>G rs28676915
NM_001130438.3(SPTAN1):c.2343C>A (p.Ala781=) rs34084388
NM_001130438.3(SPTAN1):c.237+10A>G rs746224717
NM_001130438.3(SPTAN1):c.237+335G>A
NM_001130438.3(SPTAN1):c.237+4C>T rs371350283
NM_001130438.3(SPTAN1):c.2560+47C>T rs4837284
NM_001130438.3(SPTAN1):c.2610A>G (p.Gln870=) rs138101005
NM_001130438.3(SPTAN1):c.2700C>T (p.Asn900=) rs147466898
NM_001130438.3(SPTAN1):c.2778+18G>A rs372896131
NM_001130438.3(SPTAN1):c.2778+196C>G
NM_001130438.3(SPTAN1):c.2778+20G>A rs201463905
NM_001130438.3(SPTAN1):c.2778+257G>A
NM_001130438.3(SPTAN1):c.2779-143T>C
NM_001130438.3(SPTAN1):c.2880G>A (p.Val960=) rs150731568
NM_001130438.3(SPTAN1):c.3006+100G>C
NM_001130438.3(SPTAN1):c.3051G>A (p.Pro1017=) rs140279996
NM_001130438.3(SPTAN1):c.3057G>A (p.Ala1019=) rs759833805
NM_001130438.3(SPTAN1):c.3155+153G>C
NM_001130438.3(SPTAN1):c.3186A>T (p.Val1062=) rs372807389
NM_001130438.3(SPTAN1):c.3215+15_3215+16del rs551595039
NM_001130438.3(SPTAN1):c.3300G>A (p.Ala1100=) rs2227865
NM_001130438.3(SPTAN1):c.3415-155C>T
NM_001130438.3(SPTAN1):c.3520-14C>G rs142682344
NM_001130438.3(SPTAN1):c.3520-19T>G rs373387372
NM_001130438.3(SPTAN1):c.3520-209A>G
NM_001130438.3(SPTAN1):c.3520-93A>G
NM_001130438.3(SPTAN1):c.3579+225C>T
NM_001130438.3(SPTAN1):c.3580-279C>G
NM_001130438.3(SPTAN1):c.3627+201G>A
NM_001130438.3(SPTAN1):c.3627+312C>T
NM_001130438.3(SPTAN1):c.363+144C>T
NM_001130438.3(SPTAN1):c.363+274A>G
NM_001130438.3(SPTAN1):c.3849G>A (p.Ala1283=) rs117614529
NM_001130438.3(SPTAN1):c.3912C>T (p.Pro1304=) rs143844598
NM_001130438.3(SPTAN1):c.3970C>T (p.Leu1324=) rs147233101
NM_001130438.3(SPTAN1):c.4046+4C>T rs370704701
NM_001130438.3(SPTAN1):c.4047-14G>T rs558154123
NM_001130438.3(SPTAN1):c.4116C>T (p.Thr1372=) rs148554113
NM_001130438.3(SPTAN1):c.4188G>A (p.Gln1396=) rs763156575
NM_001130438.3(SPTAN1):c.4224C>T (p.His1408=) rs200180598
NM_001130438.3(SPTAN1):c.4260T>G (p.Leu1420=) rs146150071
NM_001130438.3(SPTAN1):c.4410C>T (p.Thr1470=) rs2228951
NM_001130438.3(SPTAN1):c.4491+289G>A
NM_001130438.3(SPTAN1):c.4536C>T (p.Ile1512=) rs367772623
NM_001130438.3(SPTAN1):c.4540G>A (p.Ala1514Thr) rs145551982
NM_001130438.3(SPTAN1):c.4595+4G>T rs185925523
NM_001130438.3(SPTAN1):c.4773+13T>A rs539111821
NM_001130438.3(SPTAN1):c.4774-223A>G
NM_001130438.3(SPTAN1):c.4905+20G>A rs200959763
NM_001130438.3(SPTAN1):c.5019G>A (p.Lys1673=) rs114745823
NM_001130438.3(SPTAN1):c.5044-276G>T
NM_001130438.3(SPTAN1):c.5044-4C>T rs749484552
NM_001130438.3(SPTAN1):c.505-89C>T
NM_001130438.3(SPTAN1):c.5085= (p.Leu1695=) rs1415568
NM_001130438.3(SPTAN1):c.5149-10C>T rs587784437
NM_001130438.3(SPTAN1):c.5358-16C>T rs143969764
NM_001130438.3(SPTAN1):c.5358-214C>T
NM_001130438.3(SPTAN1):c.5406C>T (p.Thr1802=) rs2227862
NM_001130438.3(SPTAN1):c.5415G>A (p.Gln1805=) rs142964132
NM_001130438.3(SPTAN1):c.5460G>A (p.Ala1820=) rs140191388
NM_001130438.3(SPTAN1):c.5478+110C>G
NM_001130438.3(SPTAN1):c.5478+12G>A rs41275900
NM_001130438.3(SPTAN1):c.5479-41A>C rs7864187
NM_001130438.3(SPTAN1):c.5523C>T (p.Ile1841=) rs79569204
NM_001130438.3(SPTAN1):c.5552C>T (p.Ala1851Val) rs11543347
NM_001130438.3(SPTAN1):c.5775C>T (p.Thr1925=) rs140353002
NM_001130438.3(SPTAN1):c.5790C>T (p.Arg1930=) rs144435438
NM_001130438.3(SPTAN1):c.5925G>A (p.Ala1975=) rs11543345
NM_001130438.3(SPTAN1):c.6042T>G (p.Ser2014=) rs142830725
NM_001130438.3(SPTAN1):c.6111C>T (p.Gly2037=) rs139799727
NM_001130438.3(SPTAN1):c.6159C>T (p.His2053=) rs150902677
NM_001130438.3(SPTAN1):c.6183C>T (p.Ala2061=) rs775886527
NM_001130438.3(SPTAN1):c.6234C>T (p.Ala2078=) rs147132904
NM_001130438.3(SPTAN1):c.6280-27C>T rs3737308
NM_001130438.3(SPTAN1):c.6417C>T (p.Asp2139=) rs140418358
NM_001130438.3(SPTAN1):c.6498C>T (p.Arg2166=) rs72758823
NM_001130438.3(SPTAN1):c.651+219A>G
NM_001130438.3(SPTAN1):c.652-6G>A rs115815276
NM_001130438.3(SPTAN1):c.6549C>A (p.Thr2183=) rs116778543
NM_001130438.3(SPTAN1):c.6576+228G>C
NM_001130438.3(SPTAN1):c.6576+249T>C
NM_001130438.3(SPTAN1):c.6577-121C>T
NM_001130438.3(SPTAN1):c.6660C>T (p.Asn2220=) rs112955915
NM_001130438.3(SPTAN1):c.6689+17G>A rs143675512
NM_001130438.3(SPTAN1):c.6707+118A>G
NM_001130438.3(SPTAN1):c.6707+139G>A
NM_001130438.3(SPTAN1):c.6707+220G>A
NM_001130438.3(SPTAN1):c.6707+251C>A
NM_001130438.3(SPTAN1):c.6708-244C>T
NM_001130438.3(SPTAN1):c.6708-7C>T rs16930539
NM_001130438.3(SPTAN1):c.6762+10C>A rs367706466
NM_001130438.3(SPTAN1):c.6762+251dup
NM_001130438.3(SPTAN1):c.6762+288T>G
NM_001130438.3(SPTAN1):c.6960-8T>C rs140241053
NM_001130438.3(SPTAN1):c.7090C>T (p.Leu2364=) rs374893683
NM_001130438.3(SPTAN1):c.7146G>A (p.Thr2382=) rs75028792
NM_001130438.3(SPTAN1):c.7155G>A (p.Pro2385=) rs200456378
NM_001130438.3(SPTAN1):c.7161-8G>A rs202180736
NM_001130438.3(SPTAN1):c.7161-9C>T rs187613754
NM_001130438.3(SPTAN1):c.7284C>T (p.Tyr2428=) rs201348505
NM_001130438.3(SPTAN1):c.7309-12_7309-11del rs770948927
NM_001130438.3(SPTAN1):c.7359C>T (p.Tyr2453=) rs138634476
NM_001130438.3(SPTAN1):c.7365C>T (p.Asp2455=) rs142777123
NM_001130438.3(SPTAN1):c.7389C>T (p.Thr2463=) rs2228952
NM_001130438.3(SPTAN1):c.7392G>A (p.Ala2464=) rs149318543
NM_001130438.3(SPTAN1):c.7419G>A (p.Ser2473=) rs375649697
NM_001130438.3(SPTAN1):c.774G>A (p.Gln258=) rs138609094
NM_001130438.3(SPTAN1):c.785+20T>C rs529962403
NM_001130438.3(SPTAN1):c.930+17G>A rs117436936
NM_001130438.3(SPTAN1):c.931-16C>T rs149289060
NM_001130438.3(SPTAN1):c.979C>T (p.Leu327=) rs587784442

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