ClinVar Miner

List of variants in gene CNTNAP2 reported as benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
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.1659G>A (p.Ala553=) rs34592169
NM_014141.6(CNTNAP2):c.1777+10A>G rs2286127
NM_014141.6(CNTNAP2):c.2280A>G (p.Ser760=) rs10240503
NM_014141.6(CNTNAP2):c.3248-4A>G rs3779031
NM_014141.6(CNTNAP2):c.3723G>A (p.Ala1241=) rs9648691
NM_014141.6(CNTNAP2):c.551-11_551-10insG rs35167289

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