ClinVar Miner

List of variants in gene TCAP reported as likely benign for Cardiovascular phenotype

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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_003673.4(TCAP):c.32C>T (p.Ser11Leu) rs45495192 0.00113
NM_003673.4(TCAP):c.353C>T (p.Ala118Val) rs143233087 0.00092
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.132C>T (p.Asp44=) rs397516861 0.00006
NM_003673.4(TCAP):c.447C>T (p.Pro149=) rs45614332 0.00004
NM_003673.4(TCAP):c.54G>C (p.Arg18=) rs754054712 0.00004
NM_003673.4(TCAP):c.261G>T (p.Arg87=) rs375389509 0.00003
NM_003673.4(TCAP):c.87A>G (p.Thr29=) rs144741021 0.00003
NM_003673.4(TCAP):c.279C>T (p.Ile93=) rs144149447 0.00002
NM_003673.4(TCAP):c.33G>A (p.Ser11=) rs762224660 0.00002
NM_003673.4(TCAP):c.186G>A (p.Gln62=) rs1201846776 0.00001
NM_003673.4(TCAP):c.195C>G (p.Pro65=) rs370118201 0.00001
NM_003673.4(TCAP):c.24C>T (p.Cys8=) rs756548785 0.00001
NM_003673.4(TCAP):c.282C>T (p.Phe94=) rs749565002 0.00001
NM_003673.4(TCAP):c.300C>T (p.Gly100=) rs187261074 0.00001
NM_003673.4(TCAP):c.483C>T (p.Ser161=) rs1213356091 0.00001
NM_003673.4(TCAP):c.192G>A (p.Ser64=) rs771585295
NM_003673.4(TCAP):c.192G>T (p.Ser64=) rs771585295
NM_003673.4(TCAP):c.195C>T (p.Pro65=)
NM_003673.4(TCAP):c.208C>A (p.Arg70=) rs775636212
NM_003673.4(TCAP):c.216C>T (p.Gly72=)
NM_003673.4(TCAP):c.225C>A (p.Gly75=)
NM_003673.4(TCAP):c.237G>A (p.Gln79=)
NM_003673.4(TCAP):c.33G>C (p.Ser11=)
NM_003673.4(TCAP):c.346C>T (p.Leu116=) rs876657586
NM_003673.4(TCAP):c.34GAG[1] (p.Glu13del) rs397516862
NM_003673.4(TCAP):c.354G>A (p.Ala118=) rs1453601187
NM_003673.4(TCAP):c.354G>C (p.Ala118=)
NM_003673.4(TCAP):c.387C>G (p.Asp129Glu) rs768942598
NM_003673.4(TCAP):c.396G>A (p.Glu132=)
NM_003673.4(TCAP):c.51C>T (p.Arg17=)
NM_003673.4(TCAP):c.82C>T (p.Leu28=)

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