ClinVar Miner

List of variants in gene CNTNAP2 reported as uncertain significance for not specified

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Total variants: 39
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HGVS dbSNP
NM_014141.6(CNTNAP2):c.1145G>A (p.Ser382Asn) rs371839994
NM_014141.6(CNTNAP2):c.1173C>G (p.Asn391Lys) rs796052370
NM_014141.6(CNTNAP2):c.1329C>A (p.Ser443Arg) rs779881849
NM_014141.6(CNTNAP2):c.1480G>A (p.Glu494Lys) rs149032771
NM_014141.6(CNTNAP2):c.1566G>A (p.Gln522=) rs535454043
NM_014141.6(CNTNAP2):c.1566G>C (p.Gln522His) rs535454043
NM_014141.6(CNTNAP2):c.1777+7G>A rs770951811
NM_014141.6(CNTNAP2):c.1786G>A (p.Glu596Lys) rs141064983
NM_014141.6(CNTNAP2):c.1858G>A (p.Gly620Arg) rs142980731
NM_014141.6(CNTNAP2):c.2123T>C (p.Val708Ala) rs148453565
NM_014141.6(CNTNAP2):c.2238C>T (p.Asp746=) rs375648820
NM_014141.6(CNTNAP2):c.2242G>T (p.Asp748Tyr) rs371691712
NM_014141.6(CNTNAP2):c.2323A>G (p.Thr775Ala) rs1460251447
NM_014141.6(CNTNAP2):c.2340A>G (p.Ser780=) rs778124698
NM_014141.6(CNTNAP2):c.2609T>C (p.Val870Ala) rs138481453
NM_014141.6(CNTNAP2):c.2651G>A (p.Arg884Gln) rs758630057
NM_014141.6(CNTNAP2):c.2717G>A (p.Arg906His) rs759801195
NM_014141.6(CNTNAP2):c.2744G>A (p.Arg915His) rs369919189
NM_014141.6(CNTNAP2):c.2892G>A (p.Ser964=) rs148104020
NM_014141.6(CNTNAP2):c.3179C>T (p.Ala1060Val) rs369254596
NM_014141.6(CNTNAP2):c.3193C>A (p.Leu1065Ile) rs146225600
NM_014141.6(CNTNAP2):c.3235G>A (p.Val1079Ile) rs529269450
NM_014141.6(CNTNAP2):c.340C>T (p.Arg114Trp) rs756180841
NM_014141.6(CNTNAP2):c.3427G>A (p.Asp1143Asn) rs765950760
NM_014141.6(CNTNAP2):c.3559A>G (p.Ile1187Val) rs764899392
NM_014141.6(CNTNAP2):c.3595G>A (p.Ala1199Thr) rs727503878
NM_014141.6(CNTNAP2):c.3600G>A (p.Ser1200=) rs117876038
NM_014141.6(CNTNAP2):c.3675G>A (p.Ser1225=) rs142331907
NM_014141.6(CNTNAP2):c.3716-5_3716-4insCTGT rs60451214
NM_014141.6(CNTNAP2):c.3758T>C (p.Ile1253Thr) rs767821521
NM_014141.6(CNTNAP2):c.3968A>C (p.Asp1323Ala) rs142434274
NM_014141.6(CNTNAP2):c.402+8A>G rs201311931
NM_014141.6(CNTNAP2):c.479G>A (p.Arg160His) rs138738227
NM_014141.6(CNTNAP2):c.551-11T>G rs78223661
NM_014141.6(CNTNAP2):c.634A>G (p.Ile212Val) rs751076079
NM_014141.6(CNTNAP2):c.653C>T (p.Thr218Met) rs771028883
NM_014141.6(CNTNAP2):c.718C>T (p.Leu240=) rs538043826
NM_014141.6(CNTNAP2):c.806G>A (p.Ser269Asn) rs1057518565
NM_014141.6(CNTNAP2):c.857G>A (p.Arg286Gln) rs375721700

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