ClinVar Miner

List of variants in gene CNTNAP2 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 204
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HGVS dbSNP
GRCh37/hg19 7q35(chr7:146333770-146405009)x1
GRCh37/hg19 7q35(chr7:146468036-146520817)x1
GRCh37/hg19 7q35(chr7:146631506-146763340)x1
GRCh37/hg19 7q35(chr7:147516080-147803861)x1
GRCh38/hg38 7q35(chr7:146529302-146557642)x3
NM_014141.5(CNTNAP2):c.551-8dupT rs370377093
NM_014141.6(CNTNAP2):c.*1017T>G rs77001133
NM_014141.6(CNTNAP2):c.*1276_*1280dup rs369615005
NM_014141.6(CNTNAP2):c.*1433A>G rs78484397
NM_014141.6(CNTNAP2):c.*2151A>G rs28369221
NM_014141.6(CNTNAP2):c.*2665C>T rs7791181
NM_014141.6(CNTNAP2):c.*2875dup rs138367128
NM_014141.6(CNTNAP2):c.*3392C>T rs115420302
NM_014141.6(CNTNAP2):c.*3531G>A rs79360609
NM_014141.6(CNTNAP2):c.*3540G>A rs114585910
NM_014141.6(CNTNAP2):c.*3921G>A rs141005348
NM_014141.6(CNTNAP2):c.*48G>A rs78018010
NM_014141.6(CNTNAP2):c.*818dup rs145690138
NM_014141.6(CNTNAP2):c.-35G>T rs191830389
NM_014141.6(CNTNAP2):c.-46A>T rs796052368
NM_014141.6(CNTNAP2):c.1032C>T (p.Gly344=) rs142122012
NM_014141.6(CNTNAP2):c.1062G>A (p.Lys354=)
NM_014141.6(CNTNAP2):c.1068A>G (p.Leu356=) rs773110260
NM_014141.6(CNTNAP2):c.1083+16C>T rs371536143
NM_014141.6(CNTNAP2):c.1083+17G>A rs112266985
NM_014141.6(CNTNAP2):c.1083+22A>G
NM_014141.6(CNTNAP2):c.1083+282T>C
NM_014141.6(CNTNAP2):c.1083G>A (p.Val361=) rs139180845
NM_014141.6(CNTNAP2):c.1101T>C (p.Ser367=)
NM_014141.6(CNTNAP2):c.1105G>A (p.Val369Met) rs368057493
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.1145G>A (p.Ser382Asn) rs371839994
NM_014141.6(CNTNAP2):c.1165C>A (p.Arg389=) rs375172684
NM_014141.6(CNTNAP2):c.1191C>T (p.Val397=) rs1490434881
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.1335C>T (p.Ile445=) rs749205725
NM_014141.6(CNTNAP2):c.133C>T (p.His45Tyr) rs746922194
NM_014141.6(CNTNAP2):c.1349-13T>G rs1057523006
NM_014141.6(CNTNAP2):c.1349-34A>G
NM_014141.6(CNTNAP2):c.1349-8C>T
NM_014141.6(CNTNAP2):c.1377C>T (p.His459=) rs377678020
NM_014141.6(CNTNAP2):c.1455T>C (p.Asn485=) rs370095062
NM_014141.6(CNTNAP2):c.1499-293A>G
NM_014141.6(CNTNAP2):c.1566G>A (p.Gln522=) rs535454043
NM_014141.6(CNTNAP2):c.1569C>A (p.Leu523=) rs1374907989
NM_014141.6(CNTNAP2):c.1581C>T (p.Asp527=) rs774328147
NM_014141.6(CNTNAP2):c.1632C>T (p.Phe544=) rs778731812
NM_014141.6(CNTNAP2):c.1659G>A (p.Ala553=) rs34592169
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+23T>C
NM_014141.6(CNTNAP2):c.1777+7G>A rs770951811
NM_014141.6(CNTNAP2):c.1778-106A>G
NM_014141.6(CNTNAP2):c.1848T>C (p.Pro616=) rs750082302
NM_014141.6(CNTNAP2):c.1851T>C (p.Asp617=) rs150218065
NM_014141.6(CNTNAP2):c.1854C>T (p.Gly618=) rs61732849
NM_014141.6(CNTNAP2):c.1897+8T>A rs769157591
NM_014141.6(CNTNAP2):c.18C>A (p.Arg6=) rs748908765
NM_014141.6(CNTNAP2):c.1990G>A (p.Val664Ile) rs201934244
NM_014141.6(CNTNAP2):c.2043C>T (p.Tyr681=) rs779865638
NM_014141.6(CNTNAP2):c.2046C>T (p.Cys682=) rs201076428
NM_014141.6(CNTNAP2):c.2055T>C (p.Tyr685=) rs376744436
NM_014141.6(CNTNAP2):c.209-11C>T rs369056998
NM_014141.6(CNTNAP2):c.209-28_209-15del rs1064794953
NM_014141.6(CNTNAP2):c.2099-15T>C rs75858942
NM_014141.6(CNTNAP2):c.2123T>C (p.Val708Ala) rs148453565
NM_014141.6(CNTNAP2):c.2136C>T (p.Asn712=) rs187552025
NM_014141.6(CNTNAP2):c.2169T>A (p.Pro723=) rs1057522208
NM_014141.6(CNTNAP2):c.2190C>T (p.Cys730=) rs74354654
NM_014141.6(CNTNAP2):c.2255+100C>T
NM_014141.6(CNTNAP2):c.2255+259G>A
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.2295G>A (p.Leu765=) rs985931303
NM_014141.6(CNTNAP2):c.234C>T (p.Asp78=) rs757110790
NM_014141.6(CNTNAP2):c.2356G>T (p.Val786Leu) rs138517537
NM_014141.6(CNTNAP2):c.2383+15C>T rs748783925
NM_014141.6(CNTNAP2):c.2384-111A>C
NM_014141.6(CNTNAP2):c.2384-16dup rs756290919
NM_014141.6(CNTNAP2):c.2384-38G>T
NM_014141.6(CNTNAP2):c.2436C>T (p.Phe812=) rs1554474094
NM_014141.6(CNTNAP2):c.2460C>T (p.Ser820=) rs144496909
NM_014141.6(CNTNAP2):c.2508T>C (p.Phe836=) rs149185385
NM_014141.6(CNTNAP2):c.2517T>C (p.Asn839=) rs143358892
NM_014141.6(CNTNAP2):c.2541G>A (p.Lys847=)
NM_014141.6(CNTNAP2):c.2554+14G>T rs546437079
NM_014141.6(CNTNAP2):c.2554+297T>A
NM_014141.6(CNTNAP2):c.2604G>A (p.Glu868=) rs267601389
NM_014141.6(CNTNAP2):c.2606T>C (p.Ile869Thr) rs121908445
NM_014141.6(CNTNAP2):c.2609T>C (p.Val870Ala) rs138481453
NM_014141.6(CNTNAP2):c.2610A>G (p.Val870=) rs1563214691
NM_014141.6(CNTNAP2):c.2715C>A (p.Ile905=) rs771064683
NM_014141.6(CNTNAP2):c.273T>C (p.Asn91=) rs773595457
NM_014141.6(CNTNAP2):c.2774-81A>C
NM_014141.6(CNTNAP2):c.2883C>T (p.Ser961=) rs549742316
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.2928T>C (p.Asn976=) rs765953292
NM_014141.6(CNTNAP2):c.2940C>T (p.Cys980=)
NM_014141.6(CNTNAP2):c.2985A>G (p.Ala995=) rs768859093
NM_014141.6(CNTNAP2):c.3010+12C>T rs371009902
NM_014141.6(CNTNAP2):c.3010+5G>A rs373422045
NM_014141.6(CNTNAP2):c.3010+6G>A rs376708056
NM_014141.6(CNTNAP2):c.3018T>C (p.Gly1006=) rs1562998457
NM_014141.6(CNTNAP2):c.3105C>T (p.Asn1035=) rs112483670
NM_014141.6(CNTNAP2):c.3111C>T (p.Pro1037=) rs368108883
NM_014141.6(CNTNAP2):c.3132G>A (p.Pro1044=) rs761663690
NM_014141.6(CNTNAP2):c.3174C>G (p.Thr1058=) rs143226012
NM_014141.6(CNTNAP2):c.3180G>A (p.Ala1060=) rs372645983
NM_014141.6(CNTNAP2):c.3180G>C (p.Ala1060=) rs372645983
NM_014141.6(CNTNAP2):c.318C>T (p.Ser106=) rs61732853
NM_014141.6(CNTNAP2):c.3198C>T (p.Tyr1066=) rs772842467
NM_014141.6(CNTNAP2):c.3234C>T (p.Leu1078=) rs199563642
NM_014141.6(CNTNAP2):c.3247+16C>A rs370512570
NM_014141.6(CNTNAP2):c.3247+232G>A
NM_014141.6(CNTNAP2):c.3248-10T>C rs999378427
NM_014141.6(CNTNAP2):c.3248-244G>A
NM_014141.6(CNTNAP2):c.3248-4A>G rs3779031
NM_014141.6(CNTNAP2):c.3252C>T (p.Ser1084=) rs893619983
NM_014141.6(CNTNAP2):c.3305T>C (p.Val1102Ala) rs111599875
NM_014141.6(CNTNAP2):c.3345C>T (p.Val1115=) rs1060504951
NM_014141.6(CNTNAP2):c.3360C>T (p.His1120=) rs563414260
NM_014141.6(CNTNAP2):c.3402G>A (p.Val1134=) rs727503877
NM_014141.6(CNTNAP2):c.3417A>G (p.Pro1139=) rs368474520
NM_014141.6(CNTNAP2):c.341G>A (p.Arg114Gln) rs189731792
NM_014141.6(CNTNAP2):c.3426C>G (p.Ser1142=) rs749926530
NM_014141.6(CNTNAP2):c.3475+15C>T rs201902109
NM_014141.6(CNTNAP2):c.3475+16G>A rs193228886
NM_014141.6(CNTNAP2):c.3475+19A>C rs749665763
NM_014141.6(CNTNAP2):c.3475+37C>T
NM_014141.6(CNTNAP2):c.3476-15C>A rs77706740
NM_014141.6(CNTNAP2):c.3476-15_3476-12dup rs1554427506
NM_014141.6(CNTNAP2):c.3476-7C>T rs1057520468
NM_014141.6(CNTNAP2):c.348C>G (p.Leu116=) rs1344490369
NM_014141.6(CNTNAP2):c.3522A>T (p.Gly1174=) rs141078449
NM_014141.6(CNTNAP2):c.3540C>T (p.Ser1180=) rs377629345
NM_014141.6(CNTNAP2):c.354C>T (p.Ser118=) rs141831869
NM_014141.6(CNTNAP2):c.3576C>T (p.Ala1192=) rs764089965
NM_014141.6(CNTNAP2):c.3585G>A (p.Arg1195=) rs77789547
NM_014141.6(CNTNAP2):c.3594C>T (p.Asn1198=)
NM_014141.6(CNTNAP2):c.3627G>A (p.Leu1209=) rs1563066734
NM_014141.6(CNTNAP2):c.3633G>A (p.Glu1211=) rs138477292
NM_014141.6(CNTNAP2):c.3675G>A (p.Ser1225=) rs142331907
NM_014141.6(CNTNAP2):c.3678C>G (p.Ser1226=)
NM_014141.6(CNTNAP2):c.3678C>T (p.Ser1226=) rs201219937
NM_014141.6(CNTNAP2):c.3716-17TCTT[3] rs142426153
NM_014141.6(CNTNAP2):c.3716-3C>T rs773258369
NM_014141.6(CNTNAP2):c.3723G>A (p.Ala1241=) rs9648691
NM_014141.6(CNTNAP2):c.3738T>C (p.Asn1246=) rs763106283
NM_014141.6(CNTNAP2):c.3741A>C (p.Pro1247=) rs141772824
NM_014141.6(CNTNAP2):c.3783G>A (p.Ser1261=) rs778395783
NM_014141.6(CNTNAP2):c.3797-5G>C rs745770134
NM_014141.6(CNTNAP2):c.3797-6C>T rs79777576
NM_014141.6(CNTNAP2):c.3834C>T (p.Thr1278=) rs147111339
NM_014141.6(CNTNAP2):c.387A>G (p.Gln129=) rs150607716
NM_014141.6(CNTNAP2):c.3903G>A (p.Ala1301=) rs146206159
NM_014141.6(CNTNAP2):c.3918C>T (p.Ser1306=) rs774029348
NM_014141.6(CNTNAP2):c.3921G>A (p.Ala1307=) rs750224036
NM_014141.6(CNTNAP2):c.3921G>T (p.Ala1307=)
NM_014141.6(CNTNAP2):c.3924C>T (p.Asp1308=) rs766175195
NM_014141.6(CNTNAP2):c.3927C>T (p.Ala1309=) rs143856702
NM_014141.6(CNTNAP2):c.3939C>T (p.Asn1313=) rs777786908
NM_014141.6(CNTNAP2):c.3942C>T (p.Asn1314=) rs757442166
NM_014141.6(CNTNAP2):c.3968A>C (p.Asp1323Ala) rs142434274
NM_014141.6(CNTNAP2):c.3990C>G (p.Leu1330=) rs1057522590
NM_014141.6(CNTNAP2):c.3990C>T (p.Leu1330=) rs1057522590
NM_014141.6(CNTNAP2):c.402+13C>A rs532060379
NM_014141.6(CNTNAP2):c.402+8A>G rs201311931
NM_014141.6(CNTNAP2):c.515T>C (p.Ile172Thr) rs201326295
NM_014141.6(CNTNAP2):c.536A>G (p.Tyr179Cys) rs1057518820
NM_014141.6(CNTNAP2):c.551-121G>C
NM_014141.6(CNTNAP2):c.551-7G>T rs768621629
NM_014141.6(CNTNAP2):c.561T>C (p.Val187=) rs201200400
NM_014141.6(CNTNAP2):c.633C>A (p.Val211=) rs140505542
NM_014141.6(CNTNAP2):c.681C>T (p.His227=) rs142984073
NM_014141.6(CNTNAP2):c.741C>G (p.Leu247=) rs540045509
NM_014141.6(CNTNAP2):c.754+14G>C rs745882468
NM_014141.6(CNTNAP2):c.755-4G>A rs756256467
NM_014141.6(CNTNAP2):c.755-5C>A rs369675346
NM_014141.6(CNTNAP2):c.755-5C>T rs369675346
NM_014141.6(CNTNAP2):c.813G>A (p.Leu271=) rs1057522233
NM_014141.6(CNTNAP2):c.834T>C (p.Ser278=) rs61732854
NM_014141.6(CNTNAP2):c.83C>T (p.Ala28Val) rs796052366
NM_014141.6(CNTNAP2):c.849C>A (p.Arg283=) rs1057521398
NM_014141.6(CNTNAP2):c.854G>C (p.Gly285Ala) rs150918383
NM_014141.6(CNTNAP2):c.855G>A (p.Gly285=) rs372386633
NM_014141.6(CNTNAP2):c.912G>A (p.Glu304=) rs372998403
NM_014141.6(CNTNAP2):c.927C>T (p.Asp309=) rs1268578810
NM_014141.6(CNTNAP2):c.936T>C (p.Tyr312=) rs774997884
NM_014141.6(CNTNAP2):c.939+14C>T rs370916766
NM_014141.6(CNTNAP2):c.939+6T>C rs762720427
NM_014141.6(CNTNAP2):c.939+8T>A rs199994339
NM_014141.6(CNTNAP2):c.939+9G>C
NM_014141.6(CNTNAP2):c.966T>C (p.Ser322=) rs954835249
NM_014141.6(CNTNAP2):c.98-104A>G
NM_014141.6(CNTNAP2):c.98-190G>T
NM_014141.6(CNTNAP2):c.98-20T>G rs199901768
NM_014141.6(CNTNAP2):c.98-41G>A
NM_014141.6(CNTNAP2):c.9G>C (p.Ala3=) rs1237807319

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