ClinVar Miner

List of variants in gene CNTNAP2 reported as likely pathogenic for not provided

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Total variants: 6
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HGVS dbSNP
NM_014141.6(CNTNAP2):c.1651_1652del (p.Met551fs) rs1064796071
NM_014141.6(CNTNAP2):c.2096dup (p.Asp700fs) rs1554416016
NM_014141.6(CNTNAP2):c.2391T>G (p.Tyr797Ter) rs562833882
NM_014141.6(CNTNAP2):c.3382-2A>C rs1085307838
NM_014141.6(CNTNAP2):c.3657_3669dup (p.Met1224fs) rs770489662
NM_014141.6(CNTNAP2):c.778_782delinsGGGA (p.Tyr260fs) rs1554440668

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