ClinVar Miner

List of variants in gene SLC19A3 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_025243.4(SLC19A3):c.1049T>C (p.Val350Ala) rs34507036 0.09001
NM_025243.4(SLC19A3):c.435C>T (p.Ser145=) rs76517176 0.04500
NM_025243.4(SLC19A3):c.549T>C (p.Ala183=) rs74693100 0.04490
NM_025243.4(SLC19A3):c.-2-10A>G rs6728344 0.03969
NM_025243.4(SLC19A3):c.520G>A (p.Val174Ile) rs59736804 0.03276
NM_025243.4(SLC19A3):c.42C>T (p.Tyr14=) rs34080459 0.01664
NM_025243.4(SLC19A3):c.309G>A (p.Val103=) rs142837989 0.00618
NM_025243.4(SLC19A3):c.421G>A (p.Gly141Ser) rs148144444 0.00577
NM_025243.4(SLC19A3):c.621A>G (p.Ile207Met) rs145804755 0.00150
NM_025243.4(SLC19A3):c.801A>G (p.Gln267=) rs147205930 0.00067
NM_025243.4(SLC19A3):c.1132A>G (p.Ile378Val) rs117864472 0.00062
NM_025243.4(SLC19A3):c.187T>C (p.Tyr63His) rs144817990 0.00059
NM_025243.4(SLC19A3):c.18T>A (p.Thr6=) rs141093593 0.00055
NM_025243.4(SLC19A3):c.436G>A (p.Val146Ile) rs147502239 0.00036
NM_025243.4(SLC19A3):c.854G>A (p.Trp285Ter) rs373198092 0.00003
NM_025243.4(SLC19A3):c.1252C>G (p.Gln418Glu) rs368364131 0.00001
NM_025243.4(SLC19A3):c.1315-4C>A rs758218592 0.00001
NM_025243.4(SLC19A3):c.1341A>G (p.Ala447=)
NM_025243.4(SLC19A3):c.1379_1381dup (p.Ile460dup) rs756676536
NM_025243.4(SLC19A3):c.980-4del rs11334205

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