ClinVar Miner

List of variants in gene CPLANE1 reported as likely benign for not specified

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Gene type:
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Total variants: 76
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HGVS dbSNP
NM_023073.3(CPLANE1):c.*14T>C rs758449287
NM_023073.3(CPLANE1):c.*18G>T rs200332492
NM_023073.3(CPLANE1):c.1125A>G (p.Pro375=) rs61745362
NM_023073.3(CPLANE1):c.1173T>G (p.Ala391=) rs61733482
NM_023073.3(CPLANE1):c.1467C>A (p.Val489=) rs1294855346
NM_023073.3(CPLANE1):c.147G>A (p.Lys49=) rs1554117690
NM_023073.3(CPLANE1):c.1602G>A (p.Val534=) rs751572533
NM_023073.3(CPLANE1):c.1736C>T (p.Ala579Val) rs191239995
NM_023073.3(CPLANE1):c.1737G>A (p.Ala579=) rs13356183
NM_023073.3(CPLANE1):c.1755A>G (p.Ser585=) rs186970259
NM_023073.3(CPLANE1):c.1809T>C (p.Thr603=) rs115435816
NM_023073.3(CPLANE1):c.1839A>G (p.Lys613=) rs533310477
NM_023073.3(CPLANE1):c.1883G>A (p.Arg628Lys) rs74975451
NM_023073.3(CPLANE1):c.2132C>T (p.Ser711Leu) rs116237993
NM_023073.3(CPLANE1):c.2427A>G (p.Leu809=) rs886038681
NM_023073.3(CPLANE1):c.2613C>G (p.Arg871=) rs1057521941
NM_023073.3(CPLANE1):c.3240C>T (p.Ala1080=) rs28514632
NM_023073.3(CPLANE1):c.336C>T (p.Val112=) rs571875820
NM_023073.3(CPLANE1):c.3447A>G (p.Pro1149=) rs141425550
NM_023073.3(CPLANE1):c.3537T>C (p.Ala1179=) rs774018842
NM_023073.3(CPLANE1):c.3743G>A (p.Gly1248Asp) rs72736758
NM_023073.3(CPLANE1):c.378G>A (p.Gly126=) rs73750958
NM_023073.3(CPLANE1):c.3795T>A (p.Val1265=) rs74478954
NM_023073.3(CPLANE1):c.3828T>C (p.Leu1276=) rs145520487
NM_023073.3(CPLANE1):c.4080+27C>T rs78164677
NM_023073.3(CPLANE1):c.4134T>C (p.Pro1378=) rs79935028
NM_023073.3(CPLANE1):c.4310T>C (p.Ile1437Thr) rs6859950
NM_023073.3(CPLANE1):c.4403C>G (p.Ser1468Cys) rs150556877
NM_023073.3(CPLANE1):c.4460G>A (p.Ser1487Asn) rs138157520
NM_023073.3(CPLANE1):c.4481+14C>A rs903055165
NM_023073.3(CPLANE1):c.4517A>G (p.His1506Arg) rs141911199
NM_023073.3(CPLANE1):c.4698A>G (p.Leu1566=) rs143312971
NM_023073.3(CPLANE1):c.4793C>A (p.Thr1598Lys) rs147588579
NM_023073.3(CPLANE1):c.4947A>G (p.Ser1649=) rs554711652
NM_023073.3(CPLANE1):c.4954C>T (p.Leu1652=) rs141109938
NM_023073.3(CPLANE1):c.5314A>G (p.Ser1772Gly) rs79377186
NM_023073.3(CPLANE1):c.5343A>T (p.Thr1781=) rs73750949
NM_023073.3(CPLANE1):c.5381C>T (p.Pro1794Leu) rs75589774
NM_023073.3(CPLANE1):c.5421+14T>C rs753624914
NM_023073.3(CPLANE1):c.5421G>A (p.Lys1807=) rs149313666
NM_023073.3(CPLANE1):c.5512A>G (p.Thr1838Ala) rs76245173
NM_023073.3(CPLANE1):c.5571-40C>G rs10472284
NM_023073.3(CPLANE1):c.570+32G>A rs10072236
NM_023073.3(CPLANE1):c.5900+7G>T rs78315844
NM_023073.3(CPLANE1):c.5901-3T>C rs10805625
NM_023073.3(CPLANE1):c.5928G>A (p.Gly1976=) rs34161326
NM_023073.3(CPLANE1):c.6051T>C (p.Ala2017=) rs61746147
NM_023073.3(CPLANE1):c.6098T>G (p.Phe2033Cys) rs10076911
NM_023073.3(CPLANE1):c.6328A>G (p.Asn2110Asp) rs139528477
NM_023073.3(CPLANE1):c.6427A>G (p.Ile2143Val) rs6884652
NM_023073.3(CPLANE1):c.662T>C (p.Val221Ala) rs370118778
NM_023073.3(CPLANE1):c.6905C>T (p.Thr2302Met) rs34737149
NM_023073.3(CPLANE1):c.7080G>A (p.Pro2360=) rs769298457
NM_023073.3(CPLANE1):c.7234-7C>G rs141575785
NM_023073.3(CPLANE1):c.7275G>A (p.Ala2425=) rs137899908
NM_023073.3(CPLANE1):c.7428G>T (p.Leu2476=) rs145750519
NM_023073.3(CPLANE1):c.765A>C (p.Gly255=) rs117995360
NM_023073.3(CPLANE1):c.7775C>T (p.Pro2592Leu) rs16903518
NM_023073.3(CPLANE1):c.7866C>T (p.Ser2622=) rs141486731
NM_023073.3(CPLANE1):c.7958-6A>G rs373606578
NM_023073.3(CPLANE1):c.8013A>C (p.Ala2671=) rs201122718
NM_023073.3(CPLANE1):c.81+20C>T rs6876576
NM_023073.3(CPLANE1):c.8124C>T (p.Asp2708=) rs114126795
NM_023073.3(CPLANE1):c.8130G>A (p.Gln2710=) rs766837329
NM_023073.3(CPLANE1):c.8182C>A (p.Pro2728Thr) rs77014998
NM_023073.3(CPLANE1):c.82-16A>G rs1169604326
NM_023073.3(CPLANE1):c.8439C>G (p.Ser2813=) rs754005437
NM_023073.3(CPLANE1):c.8502-3A>T rs58401892
NM_023073.3(CPLANE1):c.8577C>T (p.Asp2859=) rs376535591
NM_023073.3(CPLANE1):c.8617A>G (p.Met2873Val) rs143626904
NM_023073.3(CPLANE1):c.8796+4A>C rs199810663
NM_023073.3(CPLANE1):c.9184G>A (p.Gly3062Arg) rs7702892
NM_023073.3(CPLANE1):c.9252G>A (p.Pro3084=) rs377707922
NM_023073.3(CPLANE1):c.938+19_938+22delGTCT rs748583943
NM_023073.3(CPLANE1):c.94G>A (p.Val32Ile) rs73750959
NM_023073.3(CPLANE1):c.994A>G (p.Met332Val) rs369404481

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