ClinVar Miner

List of variants in gene SLC19A3 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_025243.4(SLC19A3):c.*2139G>A rs554398899 0.00218
NM_025243.4(SLC19A3):c.621A>G (p.Ile207Met) rs145804755 0.00150
NM_025243.4(SLC19A3):c.-52T>C rs572061835 0.00123
NM_025243.4(SLC19A3):c.*1320C>T rs536282437 0.00113
NM_025243.4(SLC19A3):c.*1905G>A rs140032700 0.00096
NM_025243.4(SLC19A3):c.*1339C>T rs540235103 0.00090
NM_025243.4(SLC19A3):c.*2050C>T rs112640330 0.00078
NM_025243.4(SLC19A3):c.1145G>A (p.Ser382Asn) rs145288025 0.00073
NM_025243.4(SLC19A3):c.*2159G>A rs537737062 0.00071
NM_025243.4(SLC19A3):c.801A>G (p.Gln267=) rs147205930 0.00067
NM_025243.4(SLC19A3):c.*1256C>T rs191669498 0.00064
NM_025243.4(SLC19A3):c.613A>G (p.Arg205Gly) rs199558186 0.00041
NM_025243.4(SLC19A3):c.*1630G>T rs186778173 0.00031
NM_025243.4(SLC19A3):c.*1889T>C rs1040331392 0.00028
NM_025243.4(SLC19A3):c.*1121G>A rs539114374 0.00027
NM_025243.4(SLC19A3):c.*575G>A rs528139519 0.00016
NM_025243.4(SLC19A3):c.977G>T (p.Gly326Val) rs747823282 0.00016
NM_025243.4(SLC19A3):c.*204G>A rs560082192 0.00013
NM_025243.4(SLC19A3):c.*1517T>C rs575955380 0.00011
NM_025243.4(SLC19A3):c.*1818T>A rs189430957 0.00010
NM_025243.4(SLC19A3):c.*1842T>A rs561263131 0.00009
NM_025243.4(SLC19A3):c.*300G>A rs886055760 0.00009
NM_025243.4(SLC19A3):c.481T>C (p.Leu161=) rs375099581 0.00007
NM_025243.4(SLC19A3):c.*685G>A rs886055759 0.00006
NM_025243.4(SLC19A3):c.*176A>G rs886055761 0.00005
NM_025243.4(SLC19A3):c.*2129A>G rs561270970 0.00005
NM_025243.4(SLC19A3):c.*1072A>C rs886055755 0.00004
NM_025243.4(SLC19A3):c.*1264A>G rs553308770 0.00004
NM_025243.4(SLC19A3):c.*59T>C rs991975369 0.00004
NM_025243.4(SLC19A3):c.1442T>C (p.Val481Ala) rs779422483 0.00004
NM_025243.4(SLC19A3):c.*1355G>A rs1247435862 0.00003
NM_025243.4(SLC19A3):c.982G>A (p.Ala328Thr) rs764278369 0.00003
NM_025243.4(SLC19A3):c.-2-11C>A rs759915200 0.00002
NM_025243.4(SLC19A3):c.259G>T (p.Gly87Cys) rs200102807 0.00002
NM_025243.4(SLC19A3):c.*1059C>G rs886055756 0.00001
NM_025243.4(SLC19A3):c.*106A>G rs886055762 0.00001
NM_025243.4(SLC19A3):c.*289A>G rs1695043276 0.00001
NM_025243.4(SLC19A3):c.1412A>G (p.Gln471Arg) rs1201780335 0.00001
NM_025243.4(SLC19A3):c.1439A>G (p.Asp480Gly) rs754918776 0.00001
NM_025243.4(SLC19A3):c.1463G>C (p.Ser488Thr) rs540774490 0.00001
NM_025243.4(SLC19A3):c.861C>T (p.Phe287=) rs764867524 0.00001
NM_025243.4(SLC19A3):c.*1003G>T rs886055757
NM_025243.4(SLC19A3):c.*1044G>A rs1695015092
NM_025243.4(SLC19A3):c.*1104T>C rs886055754
NM_025243.4(SLC19A3):c.*1207C>T rs1427276202
NM_025243.4(SLC19A3):c.*1463G>A rs555334820
NM_025243.4(SLC19A3):c.*2033A>G rs886055753
NM_025243.4(SLC19A3):c.*2130_*2132delinsCGC rs386655913
NM_025243.4(SLC19A3):c.*33A>G rs886055763
NM_025243.4(SLC19A3):c.*570T>A rs1461906570
NM_025243.4(SLC19A3):c.*591ATT[2] rs539344508
NM_025243.4(SLC19A3):c.*713C>T rs1574539152
NM_025243.4(SLC19A3):c.*778G>C rs886055758
NM_025243.4(SLC19A3):c.*924C>T rs957030750
NM_025243.4(SLC19A3):c.*977del rs569329913
NM_025243.4(SLC19A3):c.1204C>T (p.Arg402Cys) rs150523975
NM_025243.4(SLC19A3):c.360G>A (p.Glu120=) rs566837952
NM_025243.4(SLC19A3):c.390G>T (p.Val130=) rs376187918
NM_025243.4(SLC19A3):c.399C>G (p.Pro133=) rs138363524
NM_025243.4(SLC19A3):c.636C>A (p.Ser212Arg) rs372767819
NM_025243.4(SLC19A3):c.876T>C (p.Phe292=) rs1695549459

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