ClinVar Miner

List of variants in gene CPLANE1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_001384732.1(CPLANE1):c.5421G>A (p.Lys1807=) rs149313666 0.00495
NM_001384732.1(CPLANE1):c.8779A>G (p.Met2927Val) rs143626904 0.00200
NM_001384732.1(CPLANE1):c.8790C>T (p.Ser2930=) rs148005445 0.00167
NM_001384732.1(CPLANE1):c.1755A>G (p.Ser585=) rs186970259 0.00113
NM_001384732.1(CPLANE1):c.8711A>G (p.Asp2904Gly) rs144427399 0.00106
NM_001384732.1(CPLANE1):c.4517A>G (p.His1506Arg) rs141911199 0.00090
NM_001384732.1(CPLANE1):c.3828T>C (p.Leu1276=) rs145520487 0.00087
NM_001384732.1(CPLANE1):c.7534-5T>C rs537063282 0.00075
NM_001384732.1(CPLANE1):c.*18G>T rs200332492 0.00053
NM_001384732.1(CPLANE1):c.6328A>G (p.Asn2110Asp) rs139528477 0.00053
NM_001384732.1(CPLANE1):c.8175A>C (p.Ala2725=) rs201122718 0.00042
NM_001384732.1(CPLANE1):c.1116G>A (p.Thr372=) rs551066377 0.00041
NM_001384732.1(CPLANE1):c.7275G>A (p.Ala2425=) rs137899908 0.00035
NM_001384732.1(CPLANE1):c.3447A>G (p.Pro1149=) rs141425550 0.00024
NM_001384732.1(CPLANE1):c.1655C>T (p.Thr552Met) rs77739540 0.00014
NM_001384732.1(CPLANE1):c.420T>C (p.Leu140=) rs1056117590 0.00014
NM_001384732.1(CPLANE1):c.336C>T (p.Val112=) rs571875820 0.00012
NM_001384732.1(CPLANE1):c.4953A>G (p.Val1651=) rs373122844 0.00011
NM_001384732.1(CPLANE1):c.6695C>T (p.Ser2232Phe) rs751344423 0.00009
NM_001384732.1(CPLANE1):c.8739C>T (p.Asp2913=) rs376535591 0.00007
NM_001384732.1(CPLANE1):c.7414G>A (p.Ala2472Thr) rs866330679 0.00005
NM_001384732.1(CPLANE1):c.662T>C (p.Val221Ala) rs370118778 0.00004
NM_001384732.1(CPLANE1):c.7691-6T>C rs768225629 0.00004
NM_001384732.1(CPLANE1):c.2427A>G (p.Leu809=) rs886038681 0.00003
NM_001384732.1(CPLANE1):c.6172-3A>C rs780811930 0.00003
NM_001384732.1(CPLANE1):c.8679G>A (p.Pro2893=) rs370303703 0.00003
NM_001384732.1(CPLANE1):c.*14T>C rs758449287 0.00002
NM_001384732.1(CPLANE1):c.5421+14T>C rs753624914 0.00001
NM_001384732.1(CPLANE1):c.861A>T (p.Thr287=) rs555972529 0.00001
NM_001384732.1(CPLANE1):c.1372-84G>A
NM_001384732.1(CPLANE1):c.5551T>C (p.Ser1851Pro)
NM_001384732.1(CPLANE1):c.6996T>G (p.Ser2332=)
NM_001384732.1(CPLANE1):c.7290A>G (p.Gln2430=)
NM_001384732.1(CPLANE1):c.7722G>A (p.Leu2574=)
NM_001384732.1(CPLANE1):c.9414G>A (p.Pro3138=) rs377707922

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