ClinVar Miner

List of variants in gene SPRED1 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_152594.3(SPRED1):c.291G>A (p.Lys97=) rs7182445 0.82029
NM_152594.3(SPRED1):c.424-8C>A rs7180446 0.82015
NM_152594.3(SPRED1):c.1044T>C (p.Val348=) rs3751526 0.81965
NM_152594.3(SPRED1):c.424-18G>A rs7179118 0.23890
NM_152594.3(SPRED1):c.583-7A>G rs115970207 0.00630
NM_152594.3(SPRED1):c.926T>C (p.Val309Ala) rs114636635 0.00204
NM_152594.3(SPRED1):c.675C>T (p.Ser225=) rs144764225 0.00092
NM_152594.3(SPRED1):c.702C>G (p.Ile234Met) rs138553244 0.00074
NM_152594.3(SPRED1):c.207+15A>G rs377288061 0.00073
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874 0.00070
NM_152594.3(SPRED1):c.30C>A (p.Asn10Lys) rs201692618 0.00042
NM_152594.3(SPRED1):c.377-10A>G rs376134678 0.00026
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964 0.00017
NM_152594.3(SPRED1):c.938C>T (p.Thr313Met) rs766814966 0.00013
NM_152594.3(SPRED1):c.963G>A (p.Lys321=) rs369711772 0.00011
NM_152594.3(SPRED1):c.177T>C (p.Phe59=) rs397517871 0.00010
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475 0.00010
NM_152594.3(SPRED1):c.1192G>A (p.Asp398Asn) rs771480941 0.00009
NM_152594.3(SPRED1):c.587C>T (p.Thr196Ile) rs147474792 0.00008
NM_152594.3(SPRED1):c.1289G>C (p.Gly430Ala) rs749389617 0.00006
NM_152594.3(SPRED1):c.685-8T>C rs760690837 0.00005
NM_152594.3(SPRED1):c.32+20C>T rs374284804 0.00004
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495 0.00004
NM_152594.3(SPRED1):c.1202G>T (p.Cys401Phe) rs779058019 0.00003
NM_152594.3(SPRED1):c.306G>A (p.Thr102=) rs372791883 0.00003
NM_152594.3(SPRED1):c.42T>C (p.Tyr14=) rs764234046 0.00003
NM_152594.3(SPRED1):c.583-9G>T rs1421813002 0.00003
NM_152594.3(SPRED1):c.1282C>T (p.Arg428Cys) rs941091989 0.00002
NM_152594.3(SPRED1):c.182G>A (p.Arg61His) rs750686148 0.00002
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467 0.00002
NM_152594.3(SPRED1):c.1191C>T (p.Asp397=) rs749745659 0.00001
NM_152594.3(SPRED1):c.15G>C (p.Thr5=) rs1278027767 0.00001
NM_152594.3(SPRED1):c.170A>G (p.Asp57Gly) rs959758606 0.00001
NM_152594.3(SPRED1):c.211G>A (p.Val71Ile) rs369150309 0.00001
NM_152594.3(SPRED1):c.353G>A (p.Arg118Lys) rs373381933 0.00001
NM_152594.3(SPRED1):c.446G>A (p.Ser149Asn) rs373384814 0.00001
NM_152594.3(SPRED1):c.46C>T (p.Arg16Ter) rs1057517941 0.00001
NM_152594.3(SPRED1):c.60G>C (p.Val20=) rs367745143 0.00001
NM_152594.3(SPRED1):c.70C>T (p.Arg24Ter) rs121434313 0.00001
NM_152594.3(SPRED1):c.954A>G (p.Leu318=) rs753357510 0.00001
NM_152594.3(SPRED1):c.990T>G (p.Gly330=) rs1184835258 0.00001
NM_152594.3(SPRED1):c.-12G>C rs371200183
NM_152594.3(SPRED1):c.1087A>G (p.Ile363Val)
NM_152594.3(SPRED1):c.1112G>C (p.Cys371Ser)
NM_152594.3(SPRED1):c.1117G>C (p.Glu373Gln)
NM_152594.3(SPRED1):c.1163C>T (p.Ser388Phe) rs1888487548
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe)
NM_152594.3(SPRED1):c.1231T>C (p.Ser411Pro)
NM_152594.3(SPRED1):c.1281_*4dup (p.His427_Ter445=) rs1888490960
NM_152594.3(SPRED1):c.1299T>C (p.Cys433=) rs2141016779
NM_152594.3(SPRED1):c.1304G>A (p.Cys435Tyr)
NM_152594.3(SPRED1):c.189G>C (p.Glu63Asp) rs2140978555
NM_152594.3(SPRED1):c.221G>T (p.Cys74Phe) rs1412213561
NM_152594.3(SPRED1):c.502T>G (p.Tyr168Asp) rs1566872960
NM_152594.3(SPRED1):c.582+16A>G rs1895996789
NM_152594.3(SPRED1):c.808G>T (p.Asp270Tyr)
NM_152594.3(SPRED1):c.881A>T (p.Tyr294Phe) rs886051105
NM_152594.3(SPRED1):c.999T>C (p.Ser333=)

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