ClinVar Miner

List of variants reported for Childhood apraxia of speech by Fulgent Genetics, Fulgent Genetics

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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_014491.4(FOXP2):c.570A>G (p.Gln190=) rs61758964 0.01012
NM_014491.4(FOXP2):c.1937A>G (p.Asn646Ser) rs145154396 0.00026
NM_014491.4(FOXP2):c.598-1G>C rs752704782 0.00009
NM_014491.4(FOXP2):c.1494T>C (p.Tyr498=) rs191237950 0.00007
NM_014491.4(FOXP2):c.1856G>A (p.Ser619Asn) rs757373725 0.00003
NM_014491.4(FOXP2):c.1426C>T (p.Arg476Ter) rs1178491246
NM_014491.4(FOXP2):c.510ACA[4] (p.Gln191del) rs398124272

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