ClinVar Miner

List of variants in gene CNTNAP2 reported as benign

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Gene type:
ClinVar version:
Total variants: 151
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HGVS dbSNP
GRCh37/hg19 7q35(chr7:145996006-146325412)x1
GRCh37/hg19 7q35(chr7:146133926-146138550)x1
GRCh37/hg19 7q35(chr7:146133926-146139175)x1
GRCh37/hg19 7q35(chr7:146175409-146431210)x1
GRCh37/hg19 7q35(chr7:146222865-146254508)x3
GRCh37/hg19 7q35(chr7:146222865-146257321)x3
GRCh37/hg19 7q35(chr7:146223131-146254508)x3
GRCh37/hg19 7q35(chr7:146471401-146553618)x1
GRCh37/hg19 7q35(chr7:147011388-147012671)x1
GRCh37/hg19 7q35(chr7:147117454-147169167)x1
GRCh37/hg19 7q36.1(chr7:148069482-148076266)x0
GRCh37/hg19 7q36.1(chr7:148074379-148084632)x0
GRCh37/hg19 7q36.1(chr7:148074379-148087337)x0
GRCh37/hg19 7q36.1(chr7:148074486-148080647)x0
NM_014141.5(CNTNAP2):c.-115G>A rs2462603
NM_014141.6(CNTNAP2):c.*1059A>T rs1062071
NM_014141.6(CNTNAP2):c.*1175_*1178TCTT[1] rs72035437
NM_014141.6(CNTNAP2):c.*1187G>A rs2530312
NM_014141.6(CNTNAP2):c.*1557A>C rs3194
NM_014141.6(CNTNAP2):c.*175dup rs61125105
NM_014141.6(CNTNAP2):c.*2157A>G rs1062072
NM_014141.6(CNTNAP2):c.*279C>A rs987456
NM_014141.6(CNTNAP2):c.*2921C>T rs10243309
NM_014141.6(CNTNAP2):c.*2935_*2936del rs544152145
NM_014141.6(CNTNAP2):c.*3144A>G rs17170999
NM_014141.6(CNTNAP2):c.*3742A>G rs2530311
NM_014141.6(CNTNAP2):c.*3928C>T rs73473919
NM_014141.6(CNTNAP2):c.*3999dup rs35835723
NM_014141.6(CNTNAP2):c.*4738C>G rs10251347
NM_014141.6(CNTNAP2):c.*4797G>C rs2717829
NM_014141.6(CNTNAP2):c.*4839G>A rs10280038
NM_014141.6(CNTNAP2):c.*4934C>T rs2530310
NM_014141.6(CNTNAP2):c.*600_*603CTGA[3] rs3058181
NM_014141.6(CNTNAP2):c.*916_*920TAGTT[1] rs569195865
NM_014141.6(CNTNAP2):c.*9T>C rs539868299
NM_014141.6(CNTNAP2):c.-32C>T rs587780903
NM_014141.6(CNTNAP2):c.-49T>G rs549396215
NM_014141.6(CNTNAP2):c.1032C>T (p.Gly344=) rs142122012
NM_014141.6(CNTNAP2):c.1083+133A>G
NM_014141.6(CNTNAP2):c.1083+266C>T
NM_014141.6(CNTNAP2):c.1083G>A (p.Val361=) rs139180845
NM_014141.6(CNTNAP2):c.1084-113del
NM_014141.6(CNTNAP2):c.1119G>A (p.Thr373=) rs73471053
NM_014141.6(CNTNAP2):c.1137C>T (p.Asn379=) rs78543192
NM_014141.6(CNTNAP2):c.1140T>A (p.Ala380=) rs141439475
NM_014141.6(CNTNAP2):c.1220A>G (p.Asn407Ser) rs143877693
NM_014141.6(CNTNAP2):c.1247C>T (p.Ala416Val) rs34456867
NM_014141.6(CNTNAP2):c.1308C>T (p.Asn436=) rs79039458
NM_014141.6(CNTNAP2):c.1311C>T (p.Ile437=) rs56356283
NM_014141.6(CNTNAP2):c.1348+13T>G rs200282837
NM_014141.6(CNTNAP2):c.1455T>C (p.Asn485=) rs370095062
NM_014141.6(CNTNAP2):c.1498+117AAAC[3]
NM_014141.6(CNTNAP2):c.1498+232T>C
NM_014141.6(CNTNAP2):c.1498+242A>C
NM_014141.6(CNTNAP2):c.1499-86C>T
NM_014141.6(CNTNAP2):c.1566G>A (p.Gln522=) rs535454043
NM_014141.6(CNTNAP2):c.1659G>A (p.Ala553=) rs34592169
NM_014141.6(CNTNAP2):c.1670+168T>G
NM_014141.6(CNTNAP2):c.1710G>A (p.Ser570=) rs2286128
NM_014141.6(CNTNAP2):c.1777+10A>G rs2286127
NM_014141.6(CNTNAP2):c.1777+13T>G rs188140291
NM_014141.6(CNTNAP2):c.1777+266T>G
NM_014141.6(CNTNAP2):c.1777+54C>T
NM_014141.6(CNTNAP2):c.1777+7G>A rs770951811
NM_014141.6(CNTNAP2):c.1778-125G>A
NM_014141.6(CNTNAP2):c.1778-239A>G
NM_014141.6(CNTNAP2):c.1778-264A>C
NM_014141.6(CNTNAP2):c.1854C>T (p.Gly618=) rs61732849
NM_014141.6(CNTNAP2):c.1897+18A>G rs139242986
NM_014141.6(CNTNAP2):c.1897+202C>T
NM_014141.6(CNTNAP2):c.1897+25A>G
NM_014141.6(CNTNAP2):c.1897+89A>G
NM_014141.6(CNTNAP2):c.1898-9T>C rs372830287
NM_014141.6(CNTNAP2):c.2098+232G>T
NM_014141.6(CNTNAP2):c.2099-15T>C rs75858942
NM_014141.6(CNTNAP2):c.2190C>T (p.Cys730=) rs74354654
NM_014141.6(CNTNAP2):c.2256-271A>C
NM_014141.6(CNTNAP2):c.2256-276T>C
NM_014141.6(CNTNAP2):c.2256-6A>T rs10240482
NM_014141.6(CNTNAP2):c.2280A>G (p.Ser760=) rs10240503
NM_014141.6(CNTNAP2):c.2292C>T (p.His764=) rs143286960
NM_014141.6(CNTNAP2):c.2356G>T (p.Val786Leu) rs138517537
NM_014141.6(CNTNAP2):c.237C>T (p.Ser79=) rs145162968
NM_014141.6(CNTNAP2):c.2383+183G>A
NM_014141.6(CNTNAP2):c.2508T>C (p.Phe836=) rs149185385
NM_014141.6(CNTNAP2):c.2554+283T>A
NM_014141.6(CNTNAP2):c.2609T>C (p.Val870Ala) rs138481453
NM_014141.6(CNTNAP2):c.273T>C (p.Asn91=) rs773595457
NM_014141.6(CNTNAP2):c.2892G>A (p.Ser964=) rs148104020
NM_014141.6(CNTNAP2):c.2895C>A (p.Gly965=) rs75688908
NM_014141.6(CNTNAP2):c.3010+100T>C
NM_014141.6(CNTNAP2):c.3011-11C>T rs201397443
NM_014141.6(CNTNAP2):c.3105C>T (p.Asn1035=) rs112483670
NM_014141.6(CNTNAP2):c.3174C>G (p.Thr1058=) rs143226012
NM_014141.6(CNTNAP2):c.318C>T (p.Ser106=) rs61732853
NM_014141.6(CNTNAP2):c.3247+15A>G rs201602527
NM_014141.6(CNTNAP2):c.3247+16C>T rs370512570
NM_014141.6(CNTNAP2):c.3247+269T>G
NM_014141.6(CNTNAP2):c.3248-17T>A rs199753492
NM_014141.6(CNTNAP2):c.3248-4A>G rs3779031
NM_014141.6(CNTNAP2):c.3381+17A>C rs3779032
NM_014141.6(CNTNAP2):c.3381+20T>C rs587780902
NM_014141.6(CNTNAP2):c.3382-7C>T rs189589051
NM_014141.6(CNTNAP2):c.3475+159A>G
NM_014141.6(CNTNAP2):c.3476-144C>T
NM_014141.6(CNTNAP2):c.3476-15C>A rs77706740
NM_014141.6(CNTNAP2):c.3476-242T>C
NM_014141.6(CNTNAP2):c.3476-278C>T
NM_014141.6(CNTNAP2):c.3476-94T>G
NM_014141.6(CNTNAP2):c.3522A>T (p.Gly1174=) rs141078449
NM_014141.6(CNTNAP2):c.3585G>A (p.Arg1195=) rs77789547
NM_014141.6(CNTNAP2):c.3600G>A (p.Ser1200=) rs117876038
NM_014141.6(CNTNAP2):c.3633G>A (p.Glu1211=) rs138477292
NM_014141.6(CNTNAP2):c.3654G>A (p.Pro1218=) rs141764220
NM_014141.6(CNTNAP2):c.3660C>A (p.Thr1220=) rs573467341
NM_014141.6(CNTNAP2):c.3675G>A (p.Ser1225=) rs142331907
NM_014141.6(CNTNAP2):c.3678C>T (p.Ser1226=) rs201219937
NM_014141.6(CNTNAP2):c.3716-17TCTT[3] rs142426153
NM_014141.6(CNTNAP2):c.3716-5_3716-4insGT rs60451214
NM_014141.6(CNTNAP2):c.3716-6C>G rs77025884
NM_014141.6(CNTNAP2):c.3716-6delinsTTCTG rs71188981
NM_014141.6(CNTNAP2):c.3716-7_3716-6insTT rs72268642
NM_014141.6(CNTNAP2):c.3723G>A (p.Ala1241=) rs9648691
NM_014141.6(CNTNAP2):c.3741A>C (p.Pro1247=) rs141772824
NM_014141.6(CNTNAP2):c.3796+191A>G
NM_014141.6(CNTNAP2):c.3796+88G>A
NM_014141.6(CNTNAP2):c.3796+91T>C
NM_014141.6(CNTNAP2):c.3797-101G>C
NM_014141.6(CNTNAP2):c.3797-275T>C
NM_014141.6(CNTNAP2):c.3797-61A>T
NM_014141.6(CNTNAP2):c.3797-6C>T rs79777576
NM_014141.6(CNTNAP2):c.3927C>T (p.Ala1309=) rs143856702
NM_014141.6(CNTNAP2):c.402+132T>C
NM_014141.6(CNTNAP2):c.402+8A>G rs201311931
NM_014141.6(CNTNAP2):c.403-148A>G
NM_014141.6(CNTNAP2):c.551-11T>G rs78223661
NM_014141.6(CNTNAP2):c.551-11_551-10insG rs35167289
NM_014141.6(CNTNAP2):c.551-185C>T
NM_014141.6(CNTNAP2):c.561T>C (p.Val187=) rs201200400
NM_014141.6(CNTNAP2):c.681C>T (p.His227=) rs142984073
NM_014141.6(CNTNAP2):c.755-147G>T
NM_014141.6(CNTNAP2):c.755-188A>T
NM_014141.6(CNTNAP2):c.755-258C>A
NM_014141.6(CNTNAP2):c.755-5C>T rs369675346
NM_014141.6(CNTNAP2):c.834T>C (p.Ser278=) rs61732854
NM_014141.6(CNTNAP2):c.837G>A (p.Val279=) rs143507886
NM_014141.6(CNTNAP2):c.854G>C (p.Gly285Ala) rs150918383
NM_014141.6(CNTNAP2):c.939+142C>A
NM_014141.6(CNTNAP2):c.940-17A>T rs374812409
NM_014141.6(CNTNAP2):c.98-19_98-16del rs796052367
NM_014141.6(CNTNAP2):c.98-279C>A

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