ClinVar Miner

List of variants in gene SPRED1 reported as benign for cardiomyopathy

Included ClinVar conditions (519):
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Gene type:
ClinVar version:
Total variants: 40
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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.684+49_684+50insTT rs61670754 0.81547
NM_152594.3(SPRED1):c.*4662T>A rs10852019 0.77666
NM_152594.3(SPRED1):c.*5110C>T rs8026118 0.76725
NM_152594.3(SPRED1):c.424-18G>A rs7179118 0.23890
NM_152594.3(SPRED1):c.*3830G>A rs8039150 0.22628
NM_152594.3(SPRED1):c.*4932A>G rs16966843 0.20289
NM_152594.3(SPRED1):c.*2831G>A rs35490364 0.19653
NM_152594.3(SPRED1):c.424-98= rs7163339 0.17991
NM_152594.3(SPRED1):c.424-8= rs7180446 0.17985
NM_152594.3(SPRED1):c.*3521A>G rs11634702 0.11111
NM_152594.3(SPRED1):c.*1724A>C rs1554527 0.08749
NM_152594.3(SPRED1):c.*3996G>A rs72725364 0.08710
NM_152594.3(SPRED1):c.*248T>C rs16966842 0.04503
NM_152594.3(SPRED1):c.*256C>T rs145373657 0.01162
NM_152594.3(SPRED1):c.*3698T>G rs76527876 0.00908
NM_152594.3(SPRED1):c.-93C>T rs192699510 0.00724
NM_152594.3(SPRED1):c.583-7A>G rs115970207 0.00630
NM_152594.3(SPRED1):c.*427A>T rs185290497 0.00592
NM_152594.3(SPRED1):c.*2742G>T rs149336440 0.00260
NM_152594.3(SPRED1):c.*5398G>T rs115003524 0.00257
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.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.290A>G (p.Lys97Arg) rs556636985 0.00026
NM_152594.3(SPRED1):c.1226C>T (p.Ala409Val) rs751260227 0.00022
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964 0.00017
NM_152594.3(SPRED1):c.26A>T (p.Asp9Val) rs200157475 0.00010
NM_152594.3(SPRED1):c.32+20C>T rs374284804 0.00004
NM_152594.3(SPRED1):c.634G>A (p.Val212Ile) rs769630742 0.00004
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467 0.00002
NM_152594.3(SPRED1):c.1046G>C (p.Arg349Thr) rs1221405249 0.00001
NM_152594.3(SPRED1):c.446G>A (p.Ser149Asn) rs373384814 0.00001
NM_152594.3(SPRED1):c.*3946G>A rs8039337
NM_152594.3(SPRED1):c.1225G>T (p.Ala409Ser) rs762735151
NM_152594.3(SPRED1):c.582+22del

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