ClinVar Miner

List of variants in gene SPTAN1 reported as uncertain significance for not provided

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Gene type:
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Total variants: 87
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HGVS dbSNP
NM_001130438.2(SPTAN1):c.1040G>A (p.Arg347His) rs796053314
NM_001130438.2(SPTAN1):c.131A>G (p.Tyr44Cys) rs368482631
NM_001130438.2(SPTAN1):c.1337C>T (p.Ser446Phe) rs794727023
NM_001130438.2(SPTAN1):c.1375C>T (p.Arg459Cys) rs772281075
NM_001130438.2(SPTAN1):c.1528G>A (p.Glu510Lys) rs769320860
NM_001130438.2(SPTAN1):c.1633G>T (p.Ala545Ser) rs1003067844
NM_001130438.2(SPTAN1):c.1648G>T (p.Ala550Ser) rs371178746
NM_001130438.2(SPTAN1):c.1689G>T (p.Met563Ile) rs373973880
NM_001130438.2(SPTAN1):c.1755C>G (p.Leu585=)
NM_001130438.2(SPTAN1):c.1770T>G (p.Asn590Lys) rs781048881
NM_001130438.2(SPTAN1):c.1799C>A (p.Ala600Asp) rs745720603
NM_001130438.2(SPTAN1):c.1806+4A>G rs770046688
NM_001130438.2(SPTAN1):c.1916T>C (p.Ile639Thr)
NM_001130438.2(SPTAN1):c.1949C>T (p.Ala650Val) rs1057524587
NM_001130438.2(SPTAN1):c.1954C>T (p.Arg652Cys)
NM_001130438.2(SPTAN1):c.2011+10G>A rs377437879
NM_001130438.2(SPTAN1):c.2158C>A (p.His720Asn)
NM_001130438.2(SPTAN1):c.2209A>G (p.Ile737Val) rs1129922
NM_001130438.2(SPTAN1):c.2221G>T (p.Ala741Ser) rs200241514
NM_001130438.2(SPTAN1):c.2402G>A (p.Arg801Gln) rs774283264
NM_001130438.2(SPTAN1):c.2588C>G (p.Ala863Gly) rs775545003
NM_001130438.2(SPTAN1):c.2610A>G (p.Gln870=) rs138101005
NM_001130438.2(SPTAN1):c.2666C>G (p.Ser889Cys) rs886043660
NM_001130438.2(SPTAN1):c.2746A>G (p.Thr916Ala) rs1064797353
NM_001130438.2(SPTAN1):c.2871+8T>C rs1485998372
NM_001130438.2(SPTAN1):c.2889G>A (p.Thr963=) rs34654141
NM_001130438.2(SPTAN1):c.3060C>T (p.Tyr1020=) rs530361602
NM_001130438.2(SPTAN1):c.3078C>T (p.Pro1026=) rs779993051
NM_001130438.2(SPTAN1):c.3133C>T (p.Arg1045Trp) rs794727356
NM_001130438.2(SPTAN1):c.3248G>A (p.Arg1083His) rs369611161
NM_001130438.2(SPTAN1):c.3358G>A (p.Gly1120Arg) rs748698544
NM_001130438.2(SPTAN1):c.3414+4T>C rs794727389
NM_001130438.2(SPTAN1):c.3490G>A (p.Ala1164Thr) rs796053316
NM_001130438.2(SPTAN1):c.3580-5_3580-2delCCTA rs754528571
NM_001130438.2(SPTAN1):c.361C>T (p.Arg121Trp)
NM_001130438.2(SPTAN1):c.368G>A (p.Arg123His) rs775634580
NM_001130438.2(SPTAN1):c.3720-7C>T rs773023641
NM_001130438.2(SPTAN1):c.3965G>A (p.Ser1322Asn) rs756084170
NM_001130438.2(SPTAN1):c.3974G>T (p.Gly1325Val) rs886043530
NM_001130438.2(SPTAN1):c.4309C>T (p.Arg1437Cys) rs373033857
NM_001130438.2(SPTAN1):c.4525G>A (p.Asp1509Asn) rs757714696
NM_001130438.2(SPTAN1):c.4558G>A (p.Gly1520Arg) rs374801331
NM_001130438.2(SPTAN1):c.4576C>T (p.Arg1526Cys) rs796053317
NM_001130438.2(SPTAN1):c.4580A>G (p.Asn1527Ser) rs145038571
NM_001130438.2(SPTAN1):c.4829G>A (p.Arg1610Gln)
NM_001130438.2(SPTAN1):c.4930C>G (p.Gln1644Glu) rs1312145167
NM_001130438.2(SPTAN1):c.4950A>G (p.Gln1650=) rs375199636
NM_001130438.2(SPTAN1):c.5106G>A (p.Leu1702=) rs373491498
NM_001130438.2(SPTAN1):c.5171G>T (p.Ser1724Ile) rs375195855
NM_001130438.2(SPTAN1):c.5206G>A (p.Asp1736Asn) rs148294757
NM_001130438.2(SPTAN1):c.5239A>G (p.Ile1747Val) rs780622472
NM_001130438.2(SPTAN1):c.5245G>A (p.Gly1749Arg) rs771886198
NM_001130438.2(SPTAN1):c.5400C>G (p.Asp1800Glu) rs779973472
NM_001130438.2(SPTAN1):c.5545C>T (p.Arg1849Trp) rs148402616
NM_001130438.2(SPTAN1):c.55C>T (p.Arg19Trp) rs748232676
NM_001130438.2(SPTAN1):c.5907T>C (p.Ala1969=) rs768986492
NM_001130438.2(SPTAN1):c.6014A>G (p.Lys2005Arg) rs754276364
NM_001130438.2(SPTAN1):c.6027T>G (p.Tyr2009Ter) rs1554766334
NM_001130438.2(SPTAN1):c.615T>A (p.Val205=) rs763385120
NM_001130438.2(SPTAN1):c.6208T>G (p.Trp2070Gly) rs766038302
NM_001130438.2(SPTAN1):c.6270C>A (p.His2090Gln) rs370102482
NM_001130438.2(SPTAN1):c.6275G>A (p.Arg2092His)
NM_001130438.2(SPTAN1):c.6308A>G (p.Lys2103Arg) rs796053322
NM_001130438.2(SPTAN1):c.6319G>A (p.Ala2107Thr) rs1131691448
NM_001130438.2(SPTAN1):c.6408G>C (p.Glu2136Asp) rs199930602
NM_001130438.2(SPTAN1):c.641A>G (p.Lys214Arg) rs760419507
NM_001130438.2(SPTAN1):c.6424C>T (p.Arg2142Cys) rs796053323
NM_001130438.2(SPTAN1):c.6425G>A (p.Arg2142His) rs796053324
NM_001130438.2(SPTAN1):c.6496C>T (p.Arg2166Cys) rs775190610
NM_001130438.2(SPTAN1):c.6498C>T (p.Arg2166=) rs72758823
NM_001130438.2(SPTAN1):c.6610C>T (p.Arg2204Trp) rs1057524104
NM_001130438.2(SPTAN1):c.6652C>T (p.His2218Tyr) rs886043546
NM_001130438.2(SPTAN1):c.6794G>C (p.Ser2265Thr) rs796053326
NM_001130438.2(SPTAN1):c.698_723del26 (p.Val233Glyfs) rs1554741638
NM_001130438.2(SPTAN1):c.7013+7T>C rs776507647
NM_001130438.2(SPTAN1):c.7102G>C (p.Glu2368Gln) rs796053329
NM_001130438.2(SPTAN1):c.7121C>G (p.Pro2374Arg) rs796053330
NM_001130438.2(SPTAN1):c.7161-8G>A rs202180736
NM_001130438.2(SPTAN1):c.7161-9C>T rs187613754
NM_001130438.2(SPTAN1):c.7233C>T (p.Ser2411=) rs138985089
NM_001130438.2(SPTAN1):c.7316C>T (p.Thr2439Ile)
NM_001130438.2(SPTAN1):c.7395C>T (p.Phe2465=) rs752878085
NM_001130438.2(SPTAN1):c.761C>A (p.Ala254Glu) rs794727784
NM_001130438.2(SPTAN1):c.958C>T (p.Arg320Cys) rs794727910
NM_001130438.2(SPTAN1):c.959G>A (p.Arg320His) rs140076136
NM_001130438.2:c.4458delA
NM_001130438.2:c.872del

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