ClinVar Miner

List of variants in gene CNTNAP2 reported as uncertain significance by Ambry Genetics

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Total variants: 39
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HGVS dbSNP
NM_014141.6(CNTNAP2):c.*4G>A
NM_014141.6(CNTNAP2):c.1079A>G (p.Asn360Ser) rs794727873
NM_014141.6(CNTNAP2):c.1105G>T (p.Val369Leu) rs368057493
NM_014141.6(CNTNAP2):c.1145G>A (p.Ser382Asn) rs371839994
NM_014141.6(CNTNAP2):c.1220A>G (p.Asn407Ser) rs143877693
NM_014141.6(CNTNAP2):c.136G>A (p.Val46Met) rs137924687
NM_014141.6(CNTNAP2):c.1480G>A (p.Glu494Lys) rs149032771
NM_014141.6(CNTNAP2):c.1687T>C (p.Cys563Arg)
NM_014141.6(CNTNAP2):c.1786G>A (p.Glu596Lys) rs141064983
NM_014141.6(CNTNAP2):c.1837T>C (p.Trp613Arg) rs1562998233
NM_014141.6(CNTNAP2):c.1879G>A (p.Val627Ile) rs147447659
NM_014141.6(CNTNAP2):c.1943C>T (p.Thr648Met) rs534215627
NM_014141.6(CNTNAP2):c.1999G>A (p.Ala667Thr)
NM_014141.6(CNTNAP2):c.2047G>A (p.Glu683Lys) rs372580822
NM_014141.6(CNTNAP2):c.2123T>C (p.Val708Ala) rs148453565
NM_014141.6(CNTNAP2):c.2197G>A (p.Glu733Lys) rs991842796
NM_014141.6(CNTNAP2):c.2369G>A (p.Arg790His) rs73464271
NM_014141.6(CNTNAP2):c.2689C>A (p.Gln897Lys) rs200300251
NM_014141.6(CNTNAP2):c.2968G>A (p.Asp990Asn) rs1060503572
NM_014141.6(CNTNAP2):c.3109C>T (p.Pro1037Ser)
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.3361G>C (p.Glu1121Gln) rs572154707
NM_014141.6(CNTNAP2):c.341G>A (p.Arg114Gln) rs189731792
NM_014141.6(CNTNAP2):c.3549G>C (p.Gln1183His) rs1316112335
NM_014141.6(CNTNAP2):c.3558G>C (p.Gln1186His) rs1563066657
NM_014141.6(CNTNAP2):c.3577G>A (p.Ala1193Thr) rs751491210
NM_014141.6(CNTNAP2):c.3607G>C (p.Val1203Leu)
NM_014141.6(CNTNAP2):c.3758T>C (p.Ile1253Thr) rs767821521
NM_014141.6(CNTNAP2):c.3886A>C (p.Asn1296His) rs1245295352
NM_014141.6(CNTNAP2):c.3908C>T (p.Ser1303Leu)
NM_014141.6(CNTNAP2):c.469C>G (p.Arg157Gly)
NM_014141.6(CNTNAP2):c.479G>A (p.Arg160His) rs138738227
NM_014141.6(CNTNAP2):c.512G>T (p.Arg171Leu) rs368487049
NM_014141.6(CNTNAP2):c.538G>A (p.Gly180Ser)
NM_014141.6(CNTNAP2):c.653C>T (p.Thr218Met) rs771028883
NM_014141.6(CNTNAP2):c.73G>A (p.Ala25Thr) rs200866893
NM_014141.6(CNTNAP2):c.766C>T (p.Leu256Phe)
NM_014141.6(CNTNAP2):c.848G>T (p.Arg283Leu)

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