ClinVar Miner

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

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_152594.3(SPRED1):c.423+105C>G rs1879937 0.95428
NM_152594.3(SPRED1):c.377-149G>A rs1879939 0.91751
NM_152594.3(SPRED1):c.582+52A>G rs7181472 0.90817
NM_152594.3(SPRED1):c.32+307A>C rs3938236 0.86429
NM_152594.3(SPRED1):c.423+272A>G rs8036371 0.82581
NM_152594.3(SPRED1):c.33-274A>G rs10220731 0.82218
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.424-98T>C rs7163339 0.82009
NM_152594.3(SPRED1):c.423+103C>T rs1879938 0.81979
NM_152594.3(SPRED1):c.1044T>C (p.Val348=) rs3751526 0.81965
NM_152594.3(SPRED1):c.685-206G>A rs12913526 0.81962
NM_152594.3(SPRED1):c.685-184C>T rs12914722 0.81957
NM_152594.3(SPRED1):c.684+167A>G rs10083640 0.81947
NM_152594.3(SPRED1):c.684+53_684+54insTA rs59928364 0.81573
NM_152594.3(SPRED1):c.684+49_684+50insTT rs61670754 0.81547
NM_152594.3(SPRED1):c.377-319T>C rs1916153 0.77343
NM_152594.3(SPRED1):c.424-18G>A rs7179118 0.23890
NM_152594.3(SPRED1):c.423+292G>A rs75373471 0.04647
NM_152594.3(SPRED1):c.*248T>C rs16966842 0.04503
NM_152594.3(SPRED1):c.423+52C>A rs12595839 0.03842
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.*3745A>G rs142928983 0.00080
NM_152594.3(SPRED1):c.*4472C>A rs541556786 0.00071
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.124G>A (p.Val42Ile) rs147204964 0.00017
NM_152594.3(SPRED1):c.446G>A (p.Ser149Asn) rs373384814 0.00001
GRCh37/hg19 15q14(chr15:38570091-38647695)x3
NM_152594.3(SPRED1):c.*578AT[13] rs147547509
NM_152594.3(SPRED1):c.207+37A>G rs2272105
NM_152594.3(SPRED1):c.376+279_376+291del rs3841233
NM_152594.3(SPRED1):c.684+50_684+51insAAT rs34352434
NM_152594.3(SPRED1):c.685-244G>C rs12913505

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