ClinVar Miner

List of variants in gene CNTNAP2 reported as likely benign by GeneDx

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Total variants: 102
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HGVS dbSNP
NM_014141.6(CNTNAP2):c.-35G>T rs191830389
NM_014141.6(CNTNAP2):c.-46A>T rs796052368
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.1145G>A (p.Ser382Asn) rs371839994
NM_014141.6(CNTNAP2):c.1165C>A (p.Arg389=) rs375172684
NM_014141.6(CNTNAP2):c.1220A>G (p.Asn407Ser) rs143877693
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.1499-293A>G
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.1777+23T>C
NM_014141.6(CNTNAP2):c.1778-106A>G
NM_014141.6(CNTNAP2):c.1848T>C (p.Pro616=) rs750082302
NM_014141.6(CNTNAP2):c.1897+8T>A rs769157591
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.209-11C>T rs369056998
NM_014141.6(CNTNAP2):c.209-28_209-15del rs1064794953
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.2255+100C>T
NM_014141.6(CNTNAP2):c.2255+259G>A
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.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.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.2774-81A>C
NM_014141.6(CNTNAP2):c.2883C>T (p.Ser961=) rs549742316
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+5G>A rs373422045
NM_014141.6(CNTNAP2):c.3010+6G>A rs376708056
NM_014141.6(CNTNAP2):c.3132G>A (p.Pro1044=) rs761663690
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.3305T>C (p.Val1102Ala) rs111599875
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.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.3476-15_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.3540C>T (p.Ser1180=) rs377629345
NM_014141.6(CNTNAP2):c.3576C>T (p.Ala1192=) rs764089965
NM_014141.6(CNTNAP2):c.3594C>T (p.Asn1198=)
NM_014141.6(CNTNAP2):c.3716-3C>T rs773258369
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.3921G>T (p.Ala1307=)
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.3990C>T (p.Leu1330=) rs1057522590
NM_014141.6(CNTNAP2):c.402+13C>A rs532060379
NM_014141.6(CNTNAP2):c.551-121G>C
NM_014141.6(CNTNAP2):c.633C>A (p.Val211=) rs140505542
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.813G>A (p.Leu271=) rs1057522233
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.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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