ClinVar Miner

List of variants in gene AGTR1 studied for Renal tubular dysgenesis

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_000685.5(AGTR1):c.*798G>A rs380400 0.71156
NM_000685.5(AGTR1):c.573C>T (p.Leu191=) rs5182 0.40342
NM_000685.5(AGTR1):c.*86A>C rs5186 0.20976
NM_000685.5(AGTR1):c.1062A>G (p.Pro354=) rs5183 0.12761
NM_000685.5(AGTR1):c.*317G>A rs5188 0.03346
NM_000685.5(AGTR1):c.*70T>G rs5185 0.02605
NC_000003.12:g.148743014T>G rs12721273 0.01716
NM_000685.5(AGTR1):c.*135C>T rs1799870 0.01447
NM_000685.5(AGTR1):c.*461C>A rs12721276 0.01062
NM_000685.5(AGTR1):c.*93A>G rs5187 0.00946
NM_031850.3(AGTR1):c.-329G>T rs148296224 0.00429
NM_000685.5(AGTR1):c.-184C>A rs2307085 0.00399
NM_000685.5(AGTR1):c.730G>T (p.Ala244Ser) rs12721225 0.00235
NM_000685.5(AGTR1):c.193G>A (p.Val65Ile) rs111980524 0.00124
NM_000685.5(AGTR1):c.*40A>T rs56343250 0.00110
NM_000685.5(AGTR1):c.*816C>A rs530184828 0.00081
NM_000685.5(AGTR1):c.308T>C (p.Ile103Thr) rs145708722 0.00075
NM_000685.5(AGTR1):c.*362G>A rs144520513 0.00068
NM_000685.5(AGTR1):c.*556T>C rs12721274 0.00064
NM_000685.5(AGTR1):c.*672G>C rs573914143 0.00033
NM_000685.5(AGTR1):c.1008G>A (p.Thr336=) rs143432118 0.00031
NM_000685.5(AGTR1):c.-16G>A rs138997091 0.00029
NM_000685.5(AGTR1):c.*335A>T rs55707609 0.00026
NM_000685.5(AGTR1):c.-239G>T rs547351627 0.00026
NM_000685.5(AGTR1):c.*178G>A rs769171204 0.00016
NM_000685.5(AGTR1):c.893A>G (p.Asn298Ser) rs368951368 0.00016
NM_000685.5(AGTR1):c.340G>A (p.Ala114Thr) rs140542820 0.00010
NM_000685.5(AGTR1):c.*229C>T rs537789164 0.00009
NM_000685.5(AGTR1):c.697C>A (p.Pro233Thr) rs151206107 0.00009
NM_000685.5(AGTR1):c.487G>A (p.Ala163Thr) rs12721226 0.00007
NM_000685.5(AGTR1):c.500G>A (p.Arg167Gln) rs200184769 0.00007
NM_000685.5(AGTR1):c.*251G>A rs886058072 0.00004
NM_000685.5(AGTR1):c.427C>A (p.Leu143Ile) rs756951904 0.00004
NM_000685.5(AGTR1):c.-331C>G rs886058068 0.00003
NM_000685.5(AGTR1):c.*593G>A rs191473323 0.00002
NM_000685.5(AGTR1):c.113T>C (p.Ile38Thr) rs751575775 0.00002
NM_000685.5(AGTR1):c.170T>C (p.Met57Thr) rs758161051 0.00002
NM_000685.5(AGTR1):c.*584C>T rs1437674870 0.00001
NM_000685.5(AGTR1):c.-48+7G>A rs941217805 0.00001
NM_000685.5(AGTR1):c.110dup (p.Ile38fs) rs387906577 0.00001
NM_000685.5(AGTR1):c.152T>C (p.Ile51Thr) rs886058069 0.00001
NM_000685.5(AGTR1):c.376C>T (p.Arg126Ter) rs397514687 0.00001
NM_000685.5(AGTR1):c.845C>T (p.Thr282Met) rs104893677 0.00001
NM_031850.3(AGTR1):c.*902A>G rs1481899061 0.00001
NM_031850.3(AGTR1):c.-339T>G rs529360494 0.00001
NM_000685.5(AGTR1):c.*432G>A rs879668265
NM_000685.5(AGTR1):c.*437G>T rs5189
NM_000685.5(AGTR1):c.*463A>G rs886058073
NM_000685.5(AGTR1):c.*48G>A rs1714957636
NM_000685.5(AGTR1):c.*883T>C rs1715007054
NM_000685.5(AGTR1):c.-115A>G rs1712763222
NM_000685.5(AGTR1):c.-227T>C rs893515670
NM_000685.5(AGTR1):c.-353C>G rs1712056842
NM_000685.5(AGTR1):c.251G>A (p.Trp84Ter) rs398122935
NM_000685.5(AGTR1):c.609T>C (p.Gly203=) rs886058070
NM_000685.5(AGTR1):c.764C>T (p.Pro255Leu) rs886058071
NM_000685.5(AGTR1):c.815G>C (p.Arg272Pro) rs1218342417
NM_000685.5(AGTR1):c.879del (p.Phe293fs) rs2107975850
NM_000685.5(AGTR1):c.942C>T (p.Leu314=) rs146357970

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