ClinVar Miner

List of variants in gene SPRED1 reported as likely benign for not provided

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_152594.3(SPRED1):c.*256C>T rs145373657 0.01162
NM_152594.3(SPRED1):c.684+133A>G rs76305448 0.01099
NM_152594.3(SPRED1):c.*3057A>G rs72725362 0.01095
NM_152594.3(SPRED1):c.-332G>A rs147075186 0.00717
NM_152594.3(SPRED1):c.*3591C>T rs147489619 0.00529
NM_152594.3(SPRED1):c.32+162G>A rs142573328 0.00345
NM_152594.3(SPRED1):c.377-201A>G rs139396722 0.00283
NM_152594.3(SPRED1):c.*3561G>A rs181980647 0.00234
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.*4471C>A rs574232846 0.00071
NM_152594.3(SPRED1):c.939G>A (p.Thr313=) rs140644874 0.00070
NM_152594.3(SPRED1):c.*3192G>A rs566065329 0.00064
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.*4304G>A rs537477031 0.00017
NM_152594.3(SPRED1):c.124G>A (p.Val42Ile) rs147204964 0.00017
NM_152594.3(SPRED1):c.376+3A>T rs775985211 0.00015
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.1176G>A (p.Ser392=) rs755223172 0.00005
NM_152594.3(SPRED1):c.685-8T>C rs760690837 0.00005
NM_152594.3(SPRED1):c.594T>C (p.Gly198=) rs756643495 0.00004
NM_152594.3(SPRED1):c.684+50A>T rs200338097 0.00003
NM_152594.3(SPRED1):c.1005C>T (p.Cys335=) rs768937237 0.00002
NM_152594.3(SPRED1):c.879G>A (p.Leu293=) rs535687467 0.00002
NM_152594.3(SPRED1):c.*5202C>T rs541213700 0.00001
NM_152594.3(SPRED1):c.384C>T (p.Pro128=) rs761058615 0.00001
NC_000015.10:g.38252630G>T rs569895675
NM_152594.3(SPRED1):c.*3647T>G rs186366365
NM_152594.3(SPRED1):c.1110C>T (p.Leu370=)
NM_152594.3(SPRED1):c.1225_1226delinsTT (p.Ala409Phe)
NM_152594.3(SPRED1):c.183T>G (p.Arg61=)
NM_152594.3(SPRED1):c.636A>C (p.Val212=) rs1057523137
NM_152594.3(SPRED1):c.933T>C (p.Phe311=) rs1057522873
NM_152594.3(SPRED1):c.939G>T (p.Thr313=) rs140644874

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