ClinVar Miner

List of variants in gene PCDH19 reported as uncertain significance for not specified

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Total variants: 18
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HGVS dbSNP
NM_001105243.1(PCDH19):c.199_207delTCGGCTCCA (p.Ser67_Pro69del) rs796052840
NM_001105243.1(PCDH19):c.2655C>T (p.Asn885=) rs193148631
NM_001105243.1(PCDH19):c.769G>C (p.Val257Leu) rs201713027
NM_001184880.1(PCDH19):c.1330A>G (p.Thr444Ala) rs201671718
NM_001184880.1(PCDH19):c.1384G>A (p.Val462Met) rs200637767
NM_001184880.1(PCDH19):c.1465T>C (p.Ser489Pro) rs1555985153
NM_001184880.1(PCDH19):c.2694C>T (p.Asp898=) rs754570811
NM_001184880.1(PCDH19):c.2798A>G (p.Asp933Gly) rs369379155
NM_001184880.1(PCDH19):c.3077C>T (p.Pro1026Leu) rs762888017
NM_001184880.1(PCDH19):c.3262G>A (p.Ala1088Thr) rs370078729
NM_001184880.1(PCDH19):c.3319C>G (p.Arg1107Gly) rs191333060
NM_001184880.1(PCDH19):c.3405A>G (p.Lys1135=) rs1555972516
NM_001184880.1(PCDH19):c.3439G>A (p.Val1147Ile) rs138771033
NM_001184880.1(PCDH19):c.408_409insCTG (p.Leu136_Glu137insLeu) rs886043865
NM_001184880.1(PCDH19):c.697G>T (p.Asp233Tyr) rs1555985482
NM_001184880.1(PCDH19):c.717C>G (p.Ser239Arg) rs199628956
NM_001184880.1(PCDH19):c.896C>T (p.Thr299Ile) rs866113078
NM_001184880.1(PCDH19):c.942G>A (p.Leu314=) rs773740606

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