ClinVar Miner

List of variants in gene MED25 studied for not provided

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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_030973.4(MED25):c.180+238T>C rs1674134 0.65229
NM_030973.4(MED25):c.180+227A>G rs1674133 0.60275
NM_030973.4(MED25):c.180+108G>C rs1674132 0.54824
NM_030973.4(MED25):c.1482+200A>G rs1290652 0.54801
NM_030973.4(MED25):c.306-27del rs5828413 0.53718
NC_000019.10:g.49818255C>G rs968388 0.27374
NM_030973.4(MED25):c.1375-55T>C rs3745480 0.27008
NC_000019.10:g.49818253C>T rs7246170 0.15330
NM_030973.4(MED25):c.1230+148C>T rs1530882 0.05823
NM_030973.4(MED25):c.1375-58A>G rs3745479 0.02762
NM_030973.4(MED25):c.165G>A (p.Thr55=) rs77400039 0.01828
NM_030973.4(MED25):c.1483-7C>T rs2017698 0.01612
NM_030973.4(MED25):c.689-27G>C rs112946131 0.01303
NM_030973.4(MED25):c.525+28G>A rs183713569 0.00874
NM_030973.4(MED25):c.1727C>G (p.Ala576Gly) rs193291405 0.00836
NM_030973.4(MED25):c.1482+19G>A rs4802632 0.00704
NM_030973.4(MED25):c.1004C>T (p.Ala335Val) rs145770066 0.00443
NM_030973.4(MED25):c.93C>T (p.Tyr31=) rs61742955 0.00394
NM_030973.4(MED25):c.2088G>A (p.Leu696=) rs371157406 0.00252
NM_030973.4(MED25):c.819+14C>T rs188257265 0.00166
NM_030973.4(MED25):c.396C>T (p.Arg132=) rs142353864 0.00125
NM_030973.4(MED25):c.354C>T (p.Leu118=) rs145574885 0.00110
NM_030973.4(MED25):c.602C>T (p.Pro201Leu) rs144354024 0.00054
NM_030973.4(MED25):c.135-6T>G rs199743509 0.00036
NM_030973.4(MED25):c.679G>A (p.Val227Met) rs369825113 0.00036
NM_030973.4(MED25):c.1095G>A (p.Pro365=) rs373128874 0.00017
NM_030973.4(MED25):c.1966C>A (p.Pro656Thr) rs199761611 0.00014
NM_030973.4(MED25):c.1438C>G (p.Leu480Val) rs148214958 0.00011
NM_030973.4(MED25):c.942C>T (p.Pro314=) rs373971747 0.00009
NM_030973.4(MED25):c.1101+4G>A rs746210338 0.00007
NM_030973.4(MED25):c.1038G>T (p.Leu346=) rs759964732 0.00006
NM_030973.4(MED25):c.418C>T (p.Arg140Trp) rs781140315 0.00006
NM_030973.4(MED25):c.1572C>T (p.Gly524=) rs559482732 0.00005
NM_030973.4(MED25):c.1335C>T (p.Pro445=) rs372191174 0.00004
NM_030973.4(MED25):c.678C>T (p.Leu226=) rs770604129 0.00003
NM_030973.4(MED25):c.1691C>T (p.Ala564Val) rs750211605 0.00002
NM_030973.4(MED25):c.769C>G (p.Leu257Val) rs1057519203 0.00002
NM_030973.4(MED25):c.1190A>G (p.Asn397Ser) rs756897347 0.00001
NM_030973.4(MED25):c.1308C>T (p.Gly436=) rs750031901 0.00001
NM_030973.4(MED25):c.135-3C>T rs750459702 0.00001
NM_030973.4(MED25):c.1678G>C (p.Gly560Arg) rs866498468 0.00001
NM_030973.4(MED25):c.2042C>T (p.Pro681Leu) rs974538844 0.00001
NM_030973.4(MED25):c.316G>A (p.Gly106Arg) rs535472885 0.00001
NM_030973.4(MED25):c.384C>T (p.Phe128=) rs1204577575 0.00001
NM_030973.4(MED25):c.395G>A (p.Arg132His) rs1441155267 0.00001
NM_030973.4(MED25):c.526C>T (p.Arg176Trp) rs757456871 0.00001
NM_030973.4(MED25):c.954C>T (p.Pro318=) rs554447029 0.00001
NM_030973.4(MED25):c.1148_1165dup (p.Gln383_Ala388dup) rs765219800
NM_030973.4(MED25):c.1165del (p.Leu389fs) rs1064795342
NM_030973.4(MED25):c.1202C>T (p.Ala401Val) rs868663771
NM_030973.4(MED25):c.1230+177C>T rs4801809
NM_030973.4(MED25):c.1275G>A (p.Arg425=)
NM_030973.4(MED25):c.150T>G (p.Gly50=) rs1600311781
NM_030973.4(MED25):c.1788A>G (p.Val596=)
NM_030973.4(MED25):c.1795_1803del (p.Ser599_Ala601del) rs764613506
NM_030973.4(MED25):c.1799G>A (p.Gly600Glu) rs1188355950
NM_030973.4(MED25):c.1807G>A (p.Gly603Arg) rs2123888223
NM_030973.4(MED25):c.1887C>T (p.Pro629=)
NM_030973.4(MED25):c.1939C>T (p.Arg647Ter) rs1555802864
NM_030973.4(MED25):c.228C>T (p.Cys76=) rs770196362
NM_030973.4(MED25):c.234C>G (p.Pro78=) rs74863643
NM_030973.4(MED25):c.23C>A (p.Pro8Gln) rs980805046
NM_030973.4(MED25):c.249A>C (p.Gln83His) rs1291395600
NM_030973.4(MED25):c.314G>A (p.Gly105Asp) rs1281336559
NM_030973.4(MED25):c.377A>T (p.Asp126Val) rs751058652
NM_030973.4(MED25):c.518T>C (p.Ile173Thr) rs781753774
NM_030973.4(MED25):c.633A>G (p.Thr211=) rs369117035
NM_030973.4(MED25):c.654G>A (p.Arg218=) rs1600324452
NM_030973.4(MED25):c.735C>T (p.Val245=)
NM_030973.4(MED25):c.801dup (p.Val268fs) rs775072432
NM_030973.4(MED25):c.908-6C>A

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