ClinVar Miner

List of variants in gene TCAP reported as uncertain significance by Ambry Genetics

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_003673.4(TCAP):c.187C>T (p.Arg63Cys) rs758048577 0.00017
NM_003673.4(TCAP):c.337C>T (p.Leu113Phe) rs372312912 0.00014
NM_003673.4(TCAP):c.209G>A (p.Arg70Gln) rs552865793 0.00012
NM_003673.4(TCAP):c.223G>A (p.Gly75Ser) rs753744791 0.00010
NM_003673.4(TCAP):c.448G>A (p.Gly150Ser) rs762850913 0.00009
NM_003673.4(TCAP):c.97C>T (p.Arg33Trp) rs145524909 0.00009
NM_003673.4(TCAP):c.226C>T (p.Arg76Cys) rs572836774 0.00006
NM_003673.4(TCAP):c.480G>A (p.Met160Ile) rs755395354 0.00006
NM_003673.4(TCAP):c.113G>T (p.Cys38Phe) rs375310569 0.00005
NM_003673.4(TCAP):c.460C>T (p.Arg154Cys) rs755539784 0.00004
NM_003673.4(TCAP):c.208C>T (p.Arg70Trp) rs775636212 0.00003
NM_003673.4(TCAP):c.70G>C (p.Glu24Gln) rs993261985 0.00003
NM_003673.4(TCAP):c.386A>G (p.Asp129Gly) rs1324156287 0.00002
NM_003673.4(TCAP):c.421C>G (p.Pro141Ala) rs45509691 0.00002
NM_003673.4(TCAP):c.171C>G (p.Cys57Trp) rs369447207 0.00001
NM_003673.4(TCAP):c.194C>T (p.Pro65Leu) rs2057250642 0.00001
NM_003673.4(TCAP):c.202A>T (p.Met68Leu) rs770133993 0.00001
NM_003673.4(TCAP):c.227G>A (p.Arg76His) rs752435787 0.00001
NM_003673.4(TCAP):c.473G>A (p.Arg158His) rs397516864 0.00001
NM_003673.4(TCAP):c.49C>T (p.Arg17Cys) rs869025530 0.00001
NM_003673.4(TCAP):c.52C>T (p.Arg18Trp) rs886038989 0.00001
NM_003673.4(TCAP):c.98G>A (p.Arg33Gln) rs1085307822 0.00001
NM_003673.4(TCAP):c.107A>G (p.Glu36Gly)
NM_003673.4(TCAP):c.126GGA[1] (p.Glu43del) rs1221886757
NM_003673.4(TCAP):c.169T>C (p.Cys57Arg) rs886042772
NM_003673.4(TCAP):c.172C>G (p.Gln58Glu)
NM_003673.4(TCAP):c.188G>A (p.Arg63His)
NM_003673.4(TCAP):c.19A>G (p.Ser7Gly)
NM_003673.4(TCAP):c.223G>T (p.Gly75Cys)
NM_003673.4(TCAP):c.263T>A (p.Val88Glu)
NM_003673.4(TCAP):c.271C>A (p.Leu91Met)
NM_003673.4(TCAP):c.305C>T (p.Thr102Ile)
NM_003673.4(TCAP):c.310GAG[1] (p.Glu105del) rs748506107
NM_003673.4(TCAP):c.313G>A (p.Glu105Lys) rs146906267
NM_003673.4(TCAP):c.317G>T (p.Arg106Leu) rs576098128
NM_003673.4(TCAP):c.330del (p.Ile111fs) rs2057251924
NM_003673.4(TCAP):c.34_48dup (p.Glu16_Arg17insGluGluAsnCysGlu)
NM_003673.4(TCAP):c.382G>C (p.Val128Leu)
NM_003673.4(TCAP):c.445C>G (p.Pro149Ala) rs932397209
NM_003673.4(TCAP):c.449G>A (p.Gly150Asp)
NM_003673.4(TCAP):c.452C>T (p.Ala151Val)
NM_003673.4(TCAP):c.452_453delinsTC (p.Ala151Val) rs2057253289
NM_003673.4(TCAP):c.460C>A (p.Arg154Ser) rs755539784
NM_003673.4(TCAP):c.466_477del (p.Leu156_Ser159del)
NM_003673.4(TCAP):c.469T>A (p.Ser157Thr)
NM_003673.4(TCAP):c.472C>T (p.Arg158Cys) rs397516863
NM_003673.4(TCAP):c.493_494del (p.Gln165fs)
NM_003673.4(TCAP):c.50G>C (p.Arg17Pro) rs750796201
NM_003673.4(TCAP):c.50_51delinsCT (p.Arg17Pro) rs1555606961
NM_003673.4(TCAP):c.94A>T (p.Thr32Ser)

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