ClinVar Miner

List of variants in gene CNTNAP2 reported as uncertain significance for See cases

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_014141.6(CNTNAP2):c.2609T>C (p.Val870Ala) rs138481453 0.00096
GRCh37/hg19 7q35(chr7:145729334-146017091)x3
GRCh37/hg19 7q35(chr7:146201149-146668571)x1
GRCh37/hg19 7q35(chr7:146267781-146620307)x1
GRCh37/hg19 7q35(chr7:146424653-146848695)x1
GRCh37/hg19 7q35(chr7:146424694-146769040)x1
GRCh37/hg19 7q35(chr7:146452776-146527985)x1
GRCh37/hg19 7q35(chr7:146478366-146596217)x1
GRCh37/hg19 7q35(chr7:146498890-146636249)x3
GRCh37/hg19 7q35(chr7:146673847-146934622)x1
GRCh37/hg19 7q35(chr7:147614180-147740163)x3
GRCh37/hg19 7q35-36.1(chr7:147731177-148189741)x3
GRCh37/hg19 7q36.1(chr7:147986528-148232245)x1
GRCh37/hg19 7q36.1(chr7:148077942-148097501)x1
GRCh38/hg38 7q35(chr7:146237454-146437866)x1
GRCh38/hg38 7q35(chr7:146372225-146496919)x1
GRCh38/hg38 7q35(chr7:146652508-146770440)x1
GRCh38/hg38 7q35(chr7:146743098-146778666)x1
GRCh38/hg38 7q35(chr7:146829009-147037760)x1
GRCh38/hg38 7q35(chr7:146884454-146966144)x3
GRCh38/hg38 7q35(chr7:146972827-147058018)x1
GRCh38/hg38 7q35(chr7:147001345-147057761)x1

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