ClinVar Miner

List of variants in gene TTC7A reported as uncertain significance for not provided

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Total variants: 26
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HGVS dbSNP gnomAD frequency
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.1447G>A (p.Gly483Arg) rs150438028 0.00166
NM_020458.4(TTC7A):c.974G>A (p.Arg325Gln) rs144971707 0.00055
NM_020458.4(TTC7A):c.794G>A (p.Arg265Gln) rs78745374 0.00015
NM_020458.4(TTC7A):c.1070C>G (p.Thr357Ser) rs200443615 0.00011
NM_020458.4(TTC7A):c.1189G>A (p.Val397Ile) rs146284515 0.00011
NM_020458.4(TTC7A):c.1093G>A (p.Val365Met) rs202176990 0.00009
NM_020458.4(TTC7A):c.806G>A (p.Arg269Gln) rs200332198 0.00009
NM_020458.4(TTC7A):c.2444C>T (p.Ala815Val) rs748142531 0.00007
NM_020458.4(TTC7A):c.208G>A (p.Ala70Thr) rs367596523 0.00004
NM_020458.4(TTC7A):c.280A>C (p.Lys94Gln) rs766411601 0.00003
NM_020458.4(TTC7A):c.1016A>G (p.Lys339Arg) rs777088531 0.00002
NM_020458.4(TTC7A):c.1978A>T (p.Met660Leu) rs375666264 0.00002
NM_020458.4(TTC7A):c.497C>T (p.Ser166Leu) rs752931401 0.00002
NM_020458.4(TTC7A):c.668C>T (p.Ser223Leu) rs267599393 0.00002
NM_020458.4(TTC7A):c.1402G>A (p.Ala468Thr) rs1191845827 0.00001
NM_020458.4(TTC7A):c.1616C>T (p.Ser539Leu) rs776906926 0.00001
NM_020458.4(TTC7A):c.2312C>T (p.Ala771Val) rs538380438 0.00001
NM_020458.4(TTC7A):c.2495C>T (p.Ala832Val) rs755985958 0.00001
NM_020458.4(TTC7A):c.1297G>T (p.Ala433Ser)
NM_020458.4(TTC7A):c.1318T>C (p.Cys440Arg)
NM_020458.4(TTC7A):c.1390T>A (p.Trp464Arg) rs1131691950
NM_020458.4(TTC7A):c.2275G>A (p.Gly759Ser) rs1422354897
NM_020458.4(TTC7A):c.2470dup (p.Gln824fs) rs768053395
NM_020458.4(TTC7A):c.2577A>C (p.Ter859Cys) rs1685001234

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