ClinVar Miner

List of variants in gene TTC7A reported as likely benign for not provided

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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_020458.4(TTC7A):c.1288-87C>A rs61155978 0.03978
NM_020458.4(TTC7A):c.1288-242C>T rs77652838 0.02016
NM_020458.4(TTC7A):c.1919+154A>G rs34868688 0.01617
NM_020458.4(TTC7A):c.1511-102G>A rs73929354 0.01265
NM_020458.4(TTC7A):c.1393-299C>G rs10205984 0.01210
NM_020458.4(TTC7A):c.1510+176G>A rs10209037 0.01076
NM_020458.4(TTC7A):c.2356-202G>A rs78575079 0.00949
NM_020458.4(TTC7A):c.2152+20T>C rs13001154 0.00805
NM_020458.4(TTC7A):c.1919+667A>G rs113150549 0.00751
NM_020458.4(TTC7A):c.517+62C>G rs118098285 0.00701
NM_020458.4(TTC7A):c.649-338C>A rs74553208 0.00578
NM_020458.4(TTC7A):c.2170C>A (p.Gln724Lys) rs140166160 0.00442
NM_020458.4(TTC7A):c.1095G>T (p.Val365=) rs113844968 0.00279
NM_020458.4(TTC7A):c.2460C>T (p.Gly820=) rs58422168 0.00272
NM_020458.4(TTC7A):c.2014T>C (p.Ser672Pro) rs149602485 0.00217
NM_020458.4(TTC7A):c.1817A>G (p.Lys606Arg) rs139010200 0.00216
NM_020458.4(TTC7A):c.2211G>A (p.Ala737=) rs142959785 0.00177
NM_020458.4(TTC7A):c.1348G>A (p.Val450Met) rs114276698 0.00136
NM_020458.4(TTC7A):c.1129C>G (p.Gln377Glu) rs117304542 0.00117
NM_020458.4(TTC7A):c.2085C>G (p.Pro695=) rs139460494 0.00095
NM_020458.4(TTC7A):c.1449G>A (p.Gly483=) rs142810509 0.00024
NM_020458.4(TTC7A):c.2496C>T (p.Ala832=) rs553994940 0.00013
NM_020458.4(TTC7A):c.849G>A (p.Ala283=) rs763190482 0.00002
NM_020458.4(TTC7A):c.2127G>A (p.Thr709=) rs759287273 0.00001
NM_020458.4(TTC7A):c.2517C>T (p.Ala839=) rs751895973 0.00001
NM_020458.4(TTC7A):c.396C>T (p.Tyr132=) rs780299149 0.00001
NM_020458.4(TTC7A):c.1008C>T (p.Tyr336=) rs587777548
NM_020458.4(TTC7A):c.1026C>T (p.Ile342=) rs151317740
NM_020458.4(TTC7A):c.437G>T (p.Arg146Leu) rs61746139
NM_020458.4(TTC7A):c.912G>C (p.Leu304=) rs1572847181

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