ClinVar Miner

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

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_004744.5(LRAT):c.*2625A>G rs77071498 0.01933
NM_004744.5(LRAT):c.*3T>G rs200942685 0.00202
NM_004744.5(LRAT):c.403G>T (p.Ala135Ser) rs139819099 0.00061
NM_004744.5(LRAT):c.398A>C (p.Lys133Thr) rs147855559 0.00031
NM_004744.5(LRAT):c.569G>A (p.Arg190His) rs770186003 0.00009
NM_004744.5(LRAT):c.80C>G (p.Ser27Trp) rs141705269 0.00007
NM_004744.5(LRAT):c.517C>T (p.Pro173Ser) rs145355018 0.00004
NM_004744.5(LRAT):c.641A>C (p.Tyr214Ser) rs1199843946 0.00004
NM_004744.5(LRAT):c.224C>T (p.Pro75Leu) rs766279892 0.00003
NM_004744.5(LRAT):c.300C>T (p.Gly100=) rs770608706 0.00003
NM_004744.5(LRAT):c.359C>G (p.Ala120Gly) rs537325942 0.00003
NM_004744.5(LRAT):c.231C>G (p.Ile77Met) rs754762928 0.00002
NM_004744.5(LRAT):c.476A>G (p.Asn159Ser) rs202066076 0.00002
NM_004744.5(LRAT):c.626C>T (p.Thr209Met) rs762455309 0.00002
NM_004744.5(LRAT):c.11C>A (p.Pro4His) rs144471673 0.00001
NM_004744.5(LRAT):c.205C>T (p.Arg69Cys) rs775838916 0.00001
NM_004744.5(LRAT):c.239C>T (p.Ala80Val) rs1251943526 0.00001
NM_004744.5(LRAT):c.244A>G (p.Thr82Ala) rs747900628 0.00001
NM_004744.5(LRAT):c.299G>A (p.Gly100Asp) rs1396648864 0.00001
NM_004744.5(LRAT):c.319A>G (p.Ser107Gly) rs532889931 0.00001
NM_004744.5(LRAT):c.583G>A (p.Val195Ile) rs200524130 0.00001
NM_004744.5(LRAT):c.628G>C (p.Gly210Arg) rs1372571084 0.00001
NM_004744.5(LRAT):c.632T>G (p.Leu211Trp) rs1460560877 0.00001
NM_004744.5(LRAT):c.89C>T (p.Ala30Val) rs1042443674 0.00001
NM_004744.5(LRAT):c.*313del rs146990234
NM_004744.5(LRAT):c.111C>G (p.Asn37Lys) rs995895723
NM_004744.5(LRAT):c.140G>T (p.Arg47Leu)
NM_004744.5(LRAT):c.147C>G (p.Asp49Glu)
NM_004744.5(LRAT):c.149T>C (p.Val50Ala) rs1384466058
NM_004744.5(LRAT):c.152T>C (p.Leu51Pro)
NM_004744.5(LRAT):c.181T>A (p.Tyr61Asn)
NM_004744.5(LRAT):c.190T>C (p.Tyr64His) rs1417030380
NM_004744.5(LRAT):c.197G>A (p.Gly66Glu) rs1560870726
NM_004744.5(LRAT):c.226G>A (p.Asp76Asn)
NM_004744.5(LRAT):c.250G>A (p.Asp84Asn)
NM_004744.5(LRAT):c.26T>C (p.Val9Ala) rs1732831177
NM_004744.5(LRAT):c.304_306del (p.Ile102del) rs1169173848
NM_004744.5(LRAT):c.314T>A (p.Val105Glu) rs774998317
NM_004744.5(LRAT):c.326G>T (p.Arg109Leu) rs2111032827
NM_004744.5(LRAT):c.346T>C (p.Phe116Leu) rs1578860322
NM_004744.5(LRAT):c.364A>G (p.Ile122Val) rs907805484
NM_004744.5(LRAT):c.374A>G (p.Asn125Ser) rs1560870996
NM_004744.5(LRAT):c.382G>C (p.Asp128His) rs1732845050
NM_004744.5(LRAT):c.384C>G (p.Asp128Glu)
NM_004744.5(LRAT):c.385G>C (p.Glu129Gln)
NM_004744.5(LRAT):c.414C>A (p.Asn138Lys)
NM_004744.5(LRAT):c.428G>T (p.Arg143Leu) rs1732846919
NM_004744.5(LRAT):c.461A>G (p.Tyr154Cys) rs1470351055
NM_004744.5(LRAT):c.46C>A (p.Leu16Met)
NM_004744.5(LRAT):c.472T>C (p.Trp158Arg)
NM_004744.5(LRAT):c.477C>A (p.Asn159Lys) rs753677274
NM_004744.5(LRAT):c.487C>G (p.His163Asp) rs1010347467
NM_004744.5(LRAT):c.497C>G (p.Thr166Ser) rs749900934
NM_004744.5(LRAT):c.49CTC[1] (p.Leu18del)
NM_004744.5(LRAT):c.531G>T (p.Gln177His) rs2111033342
NM_004744.5(LRAT):c.532T>C (p.Ser178Pro) rs1732850474
NM_004744.5(LRAT):c.541T>C (p.Phe181Leu) rs2111038131
NM_004744.5(LRAT):c.545G>A (p.Cys182Tyr) rs2111038135
NM_004744.5(LRAT):c.550A>T (p.Thr184Ser) rs892032992
NM_004744.5(LRAT):c.551C>G (p.Thr184Ser) rs1414818606
NM_004744.5(LRAT):c.557A>C (p.Lys186Thr)
NM_004744.5(LRAT):c.560T>C (p.Ile187Thr)
NM_004744.5(LRAT):c.562A>C (p.Ile188Leu) rs2111038173
NM_004744.5(LRAT):c.599T>C (p.Val200Ala) rs2111038237
NM_004744.5(LRAT):c.644C>G (p.Thr215Ser) rs754566272
NM_004744.5(LRAT):c.649C>T (p.Leu217Phe)
NM_004744.5(LRAT):c.656C>A (p.Ala219Glu)
NM_004744.5(LRAT):c.667C>A (p.Pro223Thr) rs2111038370
NM_004744.5(LRAT):c.83G>A (p.Gly28Asp)
NM_004744.5(LRAT):c.97G>A (p.Asp33Asn)
NM_004744.5(LRAT):c.99C>A (p.Asp33Glu) rs1732834528

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