ClinVar Miner

List of variants in gene CNTNAP2 reported as uncertain significance by Athena Diagnostics Inc

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Total variants: 9
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HGVS dbSNP
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.3179C>T (p.Ala1060Val) rs369254596
NM_014141.6(CNTNAP2):c.3193C>A (p.Leu1065Ile) rs146225600
NM_014141.6(CNTNAP2):c.3555C>G (p.Asn1185Lys)
NM_014141.6(CNTNAP2):c.3833C>T (p.Thr1278Ile)
NM_014141.6(CNTNAP2):c.638C>T (p.Ala213Val) rs1563079216
NM_014141.6(CNTNAP2):c.73G>A (p.Ala25Thr) rs200866893
NM_014141.6(CNTNAP2):c.755-5C>T rs369675346

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