ClinVar Miner

List of variants in gene CYP24A1 reported as benign for not provided

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NC_000020.11:g.54174247T>G rs2762943 0.94516
NM_000782.5(CYP24A1):c.450-105A>G rs2259735 0.52307
NM_000782.5(CYP24A1):c.552C>T (p.Ala184=) rs2296241 0.51337
NM_000782.5(CYP24A1):c.640+272T>C rs4809959 0.50828
NM_000782.5(CYP24A1):c.1236+198T>C rs1570669 0.42105
NM_000782.5(CYP24A1):c.543+103T>C rs6022999 0.36319
NM_000782.5(CYP24A1):c.732+230T>C rs2585429 0.35780
NM_000782.5(CYP24A1):c.733-149C>G rs2762939 0.35238
NC_000020.11:g.54153445C>T rs4811494 0.30270
NM_000782.5(CYP24A1):c.*140T>C rs4809957 0.28683
NM_000782.5(CYP24A1):c.1157+204C>T rs2296237 0.28682
NM_000782.5(CYP24A1):c.1157+178G>A rs2296238 0.28672
NM_000782.5(CYP24A1):c.1125G>A (p.Pro375=) rs2296239 0.28667
NM_000782.5(CYP24A1):c.991-66T>C rs2296240 0.28665
NM_000782.5(CYP24A1):c.991-112C>T rs6091826 0.28662
NM_000782.5(CYP24A1):c.1158-200C>T rs2274132 0.28658
NM_000782.5(CYP24A1):c.1236+24T>C rs2274130 0.28637
NM_000782.5(CYP24A1):c.1236+46T>C rs1570670 0.28633
NM_000782.5(CYP24A1):c.*715C>G rs6022987 0.27231
NM_000782.5(CYP24A1):c.990+174G>A rs6127119 0.23958
NM_000782.5(CYP24A1):c.544-179A>G rs2245153 0.21814
NM_000782.5(CYP24A1):c.990+295A>G rs2209314 0.21791
NM_000782.5(CYP24A1):c.640+58A>G rs4809960 0.19872
NM_000782.5(CYP24A1):c.*50C>T rs2762934 0.17757
NM_000782.5(CYP24A1):c.1158-180G>A rs2274131 0.17425
NM_000782.5(CYP24A1):c.733-162A>G rs6013905 0.15760
NM_000782.5(CYP24A1):c.641-66A>C rs4809958 0.13474
NM_000782.5(CYP24A1):c.744G>A (p.Thr248=) rs6068816 0.08737
NM_000782.5(CYP24A1):c.990+9G>A rs6022993 0.07682
NM_000782.5(CYP24A1):c.990+46C>A rs6091828 0.07127
NM_000782.5(CYP24A1):c.*10+198A>G rs6097809 0.07079
NM_000782.5(CYP24A1):c.449+31G>A rs59262760 0.06767
NM_000782.5(CYP24A1):c.732+231G>A rs6127120 0.05803
NM_000782.5(CYP24A1):c.-76C>T rs73913755 0.05036
NM_000782.5(CYP24A1):c.844+79T>C rs11906115 0.04787
NM_000782.5(CYP24A1):c.-400G>A rs73913757 0.04441
NM_000782.5(CYP24A1):c.1527C>T (p.Ile509=) rs61730999 0.04268
NM_000782.5(CYP24A1):c.990+44A>G rs6097816 0.03118
NM_000782.5(CYP24A1):c.1121T>C (p.Met374Thr) rs6022990 0.02863
NM_000782.5(CYP24A1):c.-94A>G rs74424092 0.01798
NM_000782.5(CYP24A1):c.234T>G (p.Gly78=) rs61755338 0.01605
NM_000782.5(CYP24A1):c.1529C>T (p.Ala510Val) rs116065115 0.00529
NM_000782.5(CYP24A1):c.733-20G>T rs182327351 0.00305
NM_000782.5(CYP24A1):c.1435-14C>T rs59241115 0.00292
NM_000782.5(CYP24A1):c.1435-16T>C rs200943520 0.00263
NM_000782.5(CYP24A1):c.604G>C (p.Asp202His) rs114579367 0.00192
NM_000782.5(CYP24A1):c.1031G>A (p.Arg344His) rs116548533 0.00154
NM_000782.5(CYP24A1):c.640+15C>G rs117685582 0.00103
NM_000782.5(CYP24A1):c.378G>A (p.Pro126=) rs116104487 0.00062
NM_000782.5(CYP24A1):c.908G>C (p.Cys303Ser) rs76747058 0.00046
NM_000782.5(CYP24A1):c.150C>T (p.Gly50=) rs566481776 0.00009
NM_000782.5(CYP24A1):c.1020C>T (p.Tyr340=) rs77764129 0.00004
NM_000782.5(CYP24A1):c.641-7A>G rs182993972 0.00004
NM_000782.5(CYP24A1):c.577C>A (p.Leu193Ile) rs377696502 0.00001
NM_000782.5(CYP24A1):c.*10+74A>G rs6097810
NM_000782.5(CYP24A1):c.-154T>G rs75209626
NM_000782.5(CYP24A1):c.114G>T (p.Pro38=) rs61749689
NM_000782.5(CYP24A1):c.1236+146G>A rs1977297
NM_000782.5(CYP24A1):c.1435-20dup
NM_000782.5(CYP24A1):c.259-105G>C rs2248137
NM_000782.5(CYP24A1):c.469C>A (p.Arg157=) rs35873579
NM_000782.5(CYP24A1):c.544-18C>T
NM_000782.5(CYP24A1):c.576G>C (p.Glu192Asp)
NM_000782.5(CYP24A1):c.633G>A (p.Ser211=) rs150102121
NM_000782.5(CYP24A1):c.733-282dup rs772562011
NM_000782.5(CYP24A1):c.991-289_991-286dup rs10689729
NM_000782.5(CYP24A1):c.991-289_991-287dup rs10689729
NM_000782.5(CYP24A1):c.991-289dup rs10689729

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