ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 153
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HGVS dbSNP gnomAD frequency
NM_018451.5(CPAP):c.163C>G (p.Pro55Ala) rs17081389 0.02639
NM_018451.5(CPAP):c.187G>C (p.Asp63His) rs7336216 0.02151
NM_018451.5(CPAP):c.2693-139T>C rs73462915 0.01352
NM_018451.5(CPAP):c.975-196G>T rs116166451 0.01208
NM_018451.5(CPAP):c.287A>G (p.His96Arg) rs61739263 0.01206
NM_018451.5(CPAP):c.2826-169A>G rs116259048 0.01017
NM_018451.5(CPAP):c.3301+197G>A rs139217245 0.00956
NM_018451.5(CPAP):c.2693-162G>A rs12872137 0.00782
NM_018451.5(CPAP):c.2692+197G>A rs192311688 0.00518
NM_018451.5(CPAP):c.1233G>A (p.Pro411=) rs112133852 0.00368
NM_018451.5(CPAP):c.2826-93C>T rs142356430 0.00310
NM_018451.5(CPAP):c.866-26T>C rs201926645 0.00262
NM_018451.5(CPAP):c.1021T>G (p.Tyr341Asp) rs143258862 0.00170
NM_018451.5(CPAP):c.175A>G (p.Thr59Ala) rs138732534 0.00157
NM_018451.5(CPAP):c.646T>C (p.Cys216Arg) rs143260721 0.00148
NM_018451.5(CPAP):c.656C>T (p.Pro219Leu) rs139844197 0.00140
NM_018451.5(CPAP):c.1960G>A (p.Ala654Thr) rs140927921 0.00121
NM_018451.5(CPAP):c.2298T>A (p.Asp766Glu) rs79951875 0.00096
NM_018451.5(CPAP):c.2571C>G (p.Ser857Arg) rs78628025 0.00094
NM_018451.5(CPAP):c.2806A>G (p.Ser936Gly) rs75008861 0.00070
NM_018451.5(CPAP):c.1410G>A (p.Pro470=) rs115628561 0.00054
NM_018451.5(CPAP):c.763A>G (p.Thr255Ala) rs150932292 0.00053
NM_018451.5(CPAP):c.2432T>A (p.Val811Asp) rs151299406 0.00050
NM_018451.5(CPAP):c.1513G>A (p.Glu505Lys) rs145679691 0.00036
NM_018451.5(CPAP):c.569-4T>C rs369506056 0.00033
NM_018451.5(CPAP):c.2852A>G (p.Gln951Arg) rs138675304 0.00021
NM_018451.5(CPAP):c.1430C>T (p.Thr477Met) rs193181742 0.00014
NM_018451.5(CPAP):c.2500C>T (p.Leu834=) rs148738982 0.00014
NM_018451.5(CPAP):c.1623C>T (p.Pro541=) rs367566036 0.00012
NM_018451.5(CPAP):c.327G>A (p.Ala109=) rs371792556 0.00012
NM_018451.5(CPAP):c.974+9C>T rs376071108 0.00012
NM_018451.5(CPAP):c.622A>G (p.Thr208Ala) rs199925549 0.00011
NM_018451.5(CPAP):c.1173G>A (p.Lys391=) rs138150382 0.00010
NM_018451.5(CPAP):c.423A>G (p.Pro141=) rs773212594 0.00007
NM_018451.5(CPAP):c.865+8A>G rs373509972 0.00006
NM_018451.5(CPAP):c.990T>C (p.Ala330=) rs148288324 0.00006
NM_018451.5(CPAP):c.1431G>A (p.Thr477=) rs371730453 0.00004
NM_018451.5(CPAP):c.2466G>A (p.Pro822=) rs375926163 0.00004
NM_018451.5(CPAP):c.2772C>T (p.Asn924=) rs758450040 0.00003
NM_018451.5(CPAP):c.3216+15G>A rs746591641 0.00003
NM_018451.5(CPAP):c.975-13T>G rs771776485 0.00003
NM_018451.5(CPAP):c.1062G>A (p.Lys354=) rs1303996186 0.00002
NM_018451.5(CPAP):c.1815A>G (p.Gln605=) rs767998216 0.00002
NM_018451.5(CPAP):c.1042T>C (p.Leu348=) rs199599993 0.00001
NM_018451.5(CPAP):c.1221C>T (p.Ser407=) rs374457770 0.00001
NM_018451.5(CPAP):c.1248T>C (p.Asp416=) rs542731735 0.00001
NM_018451.5(CPAP):c.1371G>A (p.Pro457=) rs770254231 0.00001
NM_018451.5(CPAP):c.1755T>C (p.Ala585=) rs532397259 0.00001
NM_018451.5(CPAP):c.2457T>C (p.Tyr819=) rs780573822 0.00001
NM_018451.5(CPAP):c.2991+16A>G rs199650470 0.00001
NM_018451.5(CPAP):c.3105C>T (p.Asn1035=) rs769070143 0.00001
NM_018451.5(CPAP):c.3168A>C (p.Ala1056=) rs1262295248 0.00001
NM_018451.5(CPAP):c.390G>A (p.Ala130=) rs1296030799 0.00001
NM_018451.5(CPAP):c.777G>A (p.Ala259=) rs748696673 0.00001
NM_018451.5(CPAP):c.810A>G (p.Gln270=) rs572213217 0.00001
NM_018451.5(CPAP):c.-66-314dup rs200217120
NM_018451.5(CPAP):c.1077+8A>G
NM_018451.5(CPAP):c.1078-9T>C rs760244842
NM_018451.5(CPAP):c.1119A>G (p.Gln373=)
NM_018451.5(CPAP):c.1179A>G (p.Gln393=)
NM_018451.5(CPAP):c.1272C>T (p.Thr424=)
NM_018451.5(CPAP):c.129G>A (p.Glu43=)
NM_018451.5(CPAP):c.1333A>C (p.Arg445=)
NM_018451.5(CPAP):c.1378C>T (p.Leu460=)
NM_018451.5(CPAP):c.1385G>A (p.Cys462Tyr)
NM_018451.5(CPAP):c.1404T>C (p.Leu468=)
NM_018451.5(CPAP):c.1413A>G (p.Ser471=) rs1593560644
NM_018451.5(CPAP):c.144G>A (p.Val48=)
NM_018451.5(CPAP):c.1464G>A (p.Gln488=)
NM_018451.5(CPAP):c.1515G>A (p.Glu505=)
NM_018451.5(CPAP):c.1530C>T (p.Cys510=)
NM_018451.5(CPAP):c.1533T>C (p.Asp511=)
NM_018451.5(CPAP):c.1539C>T (p.Gly513=)
NM_018451.5(CPAP):c.1575A>G (p.Arg525=)
NM_018451.5(CPAP):c.1578T>G (p.Leu526=)
NM_018451.5(CPAP):c.1602C>T (p.Ser534=)
NM_018451.5(CPAP):c.1605G>C (p.Arg535=)
NM_018451.5(CPAP):c.1662C>T (p.Asp554=) rs1177633795
NM_018451.5(CPAP):c.1836G>A (p.Arg612=)
NM_018451.5(CPAP):c.183T>C (p.Phe61=)
NM_018451.5(CPAP):c.1890C>G (p.Pro630=)
NM_018451.5(CPAP):c.1905C>T (p.Asn635=)
NM_018451.5(CPAP):c.1908C>T (p.Arg636=)
NM_018451.5(CPAP):c.1911T>C (p.Ser637=)
NM_018451.5(CPAP):c.2034C>T (p.Val678=)
NM_018451.5(CPAP):c.2037A>G (p.Gln679=)
NM_018451.5(CPAP):c.2241A>G (p.Gln747=)
NM_018451.5(CPAP):c.2295C>T (p.Ser765=)
NM_018451.5(CPAP):c.2328A>G (p.Lys776=)
NM_018451.5(CPAP):c.2337G>A (p.Glu779=)
NM_018451.5(CPAP):c.2403C>T (p.Asp801=)
NM_018451.5(CPAP):c.2415T>C (p.Asn805=)
NM_018451.5(CPAP):c.2436T>G (p.Val812=)
NM_018451.5(CPAP):c.2439T>C (p.Leu813=)
NM_018451.5(CPAP):c.2529A>T (p.Ala843=) rs2138626827
NM_018451.5(CPAP):c.2586A>G (p.Thr862=)
NM_018451.5(CPAP):c.2592G>A (p.Glu864=)
NM_018451.5(CPAP):c.2692+17T>C
NM_018451.5(CPAP):c.2692+7C>T
NM_018451.5(CPAP):c.2693-4A>T
NM_018451.5(CPAP):c.2784T>C (p.Ala928=)
NM_018451.5(CPAP):c.2790T>G (p.Leu930=)
NM_018451.5(CPAP):c.27G>A (p.Glu9=)
NM_018451.5(CPAP):c.2825+18A>G
NM_018451.5(CPAP):c.2826-11G>T
NM_018451.5(CPAP):c.2844C>T (p.Phe948=)
NM_018451.5(CPAP):c.2952A>G (p.Ala984=)
NM_018451.5(CPAP):c.2992-12_2992-6del
NM_018451.5(CPAP):c.2992-15T>C rs1954198947
NM_018451.5(CPAP):c.2992-18_2992-14del
NM_018451.5(CPAP):c.2992-18_2992-17del rs151246139
NM_018451.5(CPAP):c.2992-18del
NM_018451.5(CPAP):c.2992-22_2992-19del
NM_018451.5(CPAP):c.2992-6del rs35599563
NM_018451.5(CPAP):c.303C>T (p.Cys101=)
NM_018451.5(CPAP):c.3060A>G (p.Thr1020=)
NM_018451.5(CPAP):c.3132G>A (p.Val1044=)
NM_018451.5(CPAP):c.3189C>G (p.Leu1063=) rs760735664
NM_018451.5(CPAP):c.3216+14C>T
NM_018451.5(CPAP):c.3216+17G>A
NM_018451.5(CPAP):c.3216+17G>T
NM_018451.5(CPAP):c.3217-16A>C
NM_018451.5(CPAP):c.3217-187TG[3] rs139024899
NM_018451.5(CPAP):c.3217-6C>T
NM_018451.5(CPAP):c.3217-8T>C
NM_018451.5(CPAP):c.3234T>C (p.Phe1078=)
NM_018451.5(CPAP):c.339T>C (p.Ser113=)
NM_018451.5(CPAP):c.381A>G (p.Pro127=)
NM_018451.5(CPAP):c.438T>C (p.Leu146=)
NM_018451.5(CPAP):c.537C>T (p.Leu179=)
NM_018451.5(CPAP):c.561A>G (p.Thr187=) rs201293065
NM_018451.5(CPAP):c.569-16A>T
NM_018451.5(CPAP):c.577T>C (p.Leu193=)
NM_018451.5(CPAP):c.582G>A (p.Leu194=) rs1200554022
NM_018451.5(CPAP):c.693A>G (p.Thr231=)
NM_018451.5(CPAP):c.744T>C (p.Ala248=) rs1457110903
NM_018451.5(CPAP):c.777G>C (p.Ala259=) rs748696673
NM_018451.5(CPAP):c.804G>A (p.Gln268=)
NM_018451.5(CPAP):c.849C>T (p.Asn283=)
NM_018451.5(CPAP):c.852T>C (p.Arg284=)
NM_018451.5(CPAP):c.865+20C>T
NM_018451.5(CPAP):c.865+276G>A rs143259751
NM_018451.5(CPAP):c.866-11T>A rs372344588
NM_018451.5(CPAP):c.866-15T>G
NM_018451.5(CPAP):c.866-17C>G
NM_018451.5(CPAP):c.915A>G (p.Ala305=)
NM_018451.5(CPAP):c.974+12G>A
NM_018451.5(CPAP):c.974+14T>C
NM_018451.5(CPAP):c.974+19G>T
NM_018451.5(CPAP):c.975-12G>T
NM_018451.5(CPAP):c.975-135del rs141464543
NM_018451.5(CPAP):c.975-191G>A
NM_018451.5(CPAP):c.9G>A (p.Leu3=)

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