ClinVar Miner

List of variants in gene TCAP studied for not specified

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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_003673.4(TCAP):c.453A>C (p.Ala151=) rs1053651 0.61044
NM_003673.4(TCAP):c.453= (p.Ala151=) rs1053651 0.38956
NM_003673.4(TCAP):c.110+48C>T rs2941510 0.05382
NM_003673.4(TCAP):c.316C>T (p.Arg106Cys) rs45578741 0.00813
NM_003673.4(TCAP):c.191C>T (p.Ser64Leu) rs45458802 0.00421
NM_003673.4(TCAP):c.32C>T (p.Ser11Leu) rs45495192 0.00113
NM_003673.4(TCAP):c.313G>C (p.Glu105Gln) rs146906267 0.00051
NM_003673.4(TCAP):c.60C>G (p.Ala20=) rs146502276 0.00034
NM_003673.4(TCAP):c.458G>A (p.Arg153His) rs149585781 0.00021
NM_003673.4(TCAP):c.270G>A (p.Pro90=) rs372538567 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_003673.3(TCAP):c.-13A>G rs368175926 0.00010
NM_003673.4(TCAP):c.388C>T (p.Arg130Cys) rs374886575 0.00009
NM_003673.4(TCAP):c.132C>T (p.Asp44=) rs397516861 0.00006
NM_003673.4(TCAP):c.113G>T (p.Cys38Phe) rs375310569 0.00005
NM_003673.3(TCAP):c.-18A>G rs45550442 0.00004
NM_003673.4(TCAP):c.111-17C>T rs567350904 0.00003
NM_003673.4(TCAP):c.269C>T (p.Pro90Leu) rs727504427 0.00003
NM_003673.4(TCAP):c.16C>A (p.Leu6Met) rs201664428 0.00002
NM_003673.4(TCAP):c.267G>A (p.Leu89=) rs1419129039 0.00002
NM_003673.4(TCAP):c.279C>T (p.Ile93=) rs144149447 0.00002
NM_003673.4(TCAP):c.301G>A (p.Ala101Thr) rs727503455 0.00002
NM_003673.4(TCAP):c.386A>G (p.Asp129Gly) rs1324156287 0.00002
NM_003673.4(TCAP):c.195C>G (p.Pro65=) rs370118201 0.00001
NM_003673.4(TCAP):c.423C>T (p.Pro141=) rs1360918794 0.00001
NM_003673.4(TCAP):c.473G>A (p.Arg158His) rs397516864 0.00001
NM_003673.4(TCAP):c.110+7G>A rs886038533
NM_003673.4(TCAP):c.111-11C>T
NM_003673.4(TCAP):c.111-15dup rs397516860
NM_003673.4(TCAP):c.184C>T (p.Gln62Ter)
NM_003673.4(TCAP):c.192G>A (p.Ser64=) rs771585295
NM_003673.4(TCAP):c.313G>A (p.Glu105Lys) rs146906267
NM_003673.4(TCAP):c.341A>G (p.Gln114Arg) rs1355624192
NM_003673.4(TCAP):c.346C>T (p.Leu116=) rs876657586
NM_003673.4(TCAP):c.349C>T (p.Leu117=) rs886038534
NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del) rs397516862
NM_003673.4(TCAP):c.388C>A (p.Arg130Ser) rs374886575
NM_003673.4(TCAP):c.428T>C (p.Val143Ala) rs2145074575
NM_003673.4(TCAP):c.472C>A (p.Arg158Ser) rs397516863
NM_003673.4(TCAP):c.493C>G (p.Gln165Glu) rs397516865
NM_003673.4(TCAP):c.88C>T (p.Leu30=) rs1282445039

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