ClinVar Miner

List of variants in gene SPRED1 reported as uncertain significance by Invitae

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Total variants: 85
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HGVS dbSNP
NM_152594.3(SPRED1):c.1000C>T (p.Arg334Cys) rs765603808
NM_152594.3(SPRED1):c.1001G>A (p.Arg334His)
NM_152594.3(SPRED1):c.1006G>A (p.Val336Ile) rs373477920
NM_152594.3(SPRED1):c.1031A>G (p.His344Arg) rs376679136
NM_152594.3(SPRED1):c.1076T>A (p.Ile359Asn) rs763738243
NM_152594.3(SPRED1):c.1103G>C (p.Cys368Ser)
NM_152594.3(SPRED1):c.115C>G (p.Leu39Val) rs1555389691
NM_152594.3(SPRED1):c.1189G>A (p.Asp397Asn)
NM_152594.3(SPRED1):c.118AGC[1] (p.Ser41del)
NM_152594.3(SPRED1):c.1202G>T (p.Cys401Phe) rs779058019
NM_152594.3(SPRED1):c.1217C>T (p.Ala406Val)
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe) rs1566877075
NM_152594.3(SPRED1):c.1246T>C (p.Cys416Arg)
NM_152594.3(SPRED1):c.1280A>G (p.His427Arg)
NM_152594.3(SPRED1):c.1282C>T (p.Arg428Cys) rs941091989
NM_152594.3(SPRED1):c.1283G>A (p.Arg428His) rs369492789
NM_152594.3(SPRED1):c.1289G>C (p.Gly430Ala) rs749389617
NM_152594.3(SPRED1):c.1295C>T (p.Ala432Val) rs200871227
NM_152594.3(SPRED1):c.1298G>A (p.Cys433Tyr)
NM_152594.3(SPRED1):c.1313G>T (p.Gly438Val)
NM_152594.3(SPRED1):c.1324G>A (p.Ala442Thr)
NM_152594.3(SPRED1):c.135C>G (p.Phe45Leu) rs1595733562
NM_152594.3(SPRED1):c.149A>T (p.Gln50Leu) rs1475256958
NM_152594.3(SPRED1):c.161G>T (p.Gly54Val)
NM_152594.3(SPRED1):c.170A>G (p.Asp57Gly)
NM_152594.3(SPRED1):c.178A>G (p.Ile60Val) rs761830220
NM_152594.3(SPRED1):c.181C>T (p.Arg61Cys) rs765788978
NM_152594.3(SPRED1):c.182G>A (p.Arg61His) rs750686148
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile)
NM_152594.3(SPRED1):c.221G>T (p.Cys74Phe) rs1412213561
NM_152594.3(SPRED1):c.274T>C (p.Trp92Arg) rs1566867214
NM_152594.3(SPRED1):c.281T>C (p.Ile94Thr) rs761473300
NM_152594.3(SPRED1):c.287A>G (p.Asp96Gly) rs1555391039
NM_152594.3(SPRED1):c.29A>G (p.Asn10Ser)
NM_152594.3(SPRED1):c.302T>C (p.Leu101Pro) rs1595746820
NM_152594.3(SPRED1):c.302T>G (p.Leu101Arg) rs1595746820
NM_152594.3(SPRED1):c.305C>A (p.Thr102Lys)
NM_152594.3(SPRED1):c.305C>G (p.Thr102Arg) rs754706111
NM_152594.3(SPRED1):c.315T>G (p.Ser105Arg) rs1566867263
NM_152594.3(SPRED1):c.31G>A (p.Asp11Asn)
NM_152594.3(SPRED1):c.32+3A>T
NM_152594.3(SPRED1):c.353G>C (p.Arg118Thr)
NM_152594.3(SPRED1):c.371C>T (p.Ser124Phe)
NM_152594.3(SPRED1):c.376+3A>T rs775985211
NM_152594.3(SPRED1):c.376+9T>G rs1555391063
NM_152594.3(SPRED1):c.395A>G (p.Asn132Ser) rs1595748117
NM_152594.3(SPRED1):c.401C>G (p.Ala134Gly) rs762633609
NM_152594.3(SPRED1):c.403G>C (p.Glu135Gln) rs1595748136
NM_152594.3(SPRED1):c.406G>A (p.Gly136Arg) rs1555391158
NM_152594.3(SPRED1):c.410C>T (p.Ala137Val)
NM_152594.3(SPRED1):c.421C>A (p.Gln141Lys)
NM_152594.3(SPRED1):c.423+5G>A
NM_152594.3(SPRED1):c.423+5_423+8del
NM_152594.3(SPRED1):c.431A>G (p.Glu144Gly)
NM_152594.3(SPRED1):c.451C>G (p.Leu151Val)
NM_152594.3(SPRED1):c.462_464dup (p.His155dup)
NM_152594.3(SPRED1):c.477A>T (p.Gln159His)
NM_152594.3(SPRED1):c.487G>T (p.Val163Phe)
NM_152594.3(SPRED1):c.49G>A (p.Val17Met)
NM_152594.3(SPRED1):c.511T>C (p.Ser171Pro)
NM_152594.3(SPRED1):c.517A>G (p.Ile173Val) rs1060502504
NM_152594.3(SPRED1):c.535G>A (p.Glu179Lys)
NM_152594.3(SPRED1):c.538G>T (p.Asp180Tyr) rs1375474473
NM_152594.3(SPRED1):c.583A>T (p.Ile195Leu)
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792
NM_152594.3(SPRED1):c.640C>T (p.Arg214Trp)
NM_152594.3(SPRED1):c.641G>A (p.Arg214Gln)
NM_152594.3(SPRED1):c.659G>A (p.Cys220Tyr)
NM_152594.3(SPRED1):c.666C>A (p.Ser222Arg)
NM_152594.3(SPRED1):c.683G>A (p.Arg228Lys) rs951963194
NM_152594.3(SPRED1):c.685G>T (p.Val229Phe) rs201837340
NM_152594.3(SPRED1):c.6C>A (p.Ser2Arg)
NM_152594.3(SPRED1):c.747C>G (p.Asn249Lys)
NM_152594.3(SPRED1):c.74A>G (p.Asp25Gly) rs1057524159
NM_152594.3(SPRED1):c.770G>A (p.Arg257His)
NM_152594.3(SPRED1):c.807T>G (p.Asn269Lys) rs886041428
NM_152594.3(SPRED1):c.842A>G (p.Gln281Arg) rs1427402192
NM_152594.3(SPRED1):c.881A>T (p.Tyr294Phe) rs886051105
NM_152594.3(SPRED1):c.892G>C (p.Asp298His)
NM_152594.3(SPRED1):c.917A>G (p.Lys306Arg)
NM_152594.3(SPRED1):c.920A>G (p.Asp307Gly)
NM_152594.3(SPRED1):c.922T>A (p.Ser308Thr)
NM_152594.3(SPRED1):c.974G>A (p.Arg325Gln) rs1238094530
NM_152594.3(SPRED1):c.982G>A (p.Glu328Lys)
NM_152594.3(SPRED1):c.995G>A (p.Arg332His) rs779966392

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