ClinVar Miner

List of variants in gene MED25 studied for not specified

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Total variants: 21
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HGVS dbSNP gnomAD frequency
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.-12A>G rs114843375 0.01532
NM_030973.4(MED25):c.2031G>A (p.Ala677=) rs57854058 0.01517
NM_030973.4(MED25):c.1727C>G (p.Ala576Gly) rs193291405 0.00836
NM_030973.4(MED25):c.1794C>T (p.Ala598=) rs185100172 0.00456
NM_030973.4(MED25):c.1004C>T (p.Ala335Val) rs145770066 0.00443
NM_030973.4(MED25):c.2088G>A (p.Leu696=) rs371157406 0.00252
NM_030973.4(MED25):c.1675-7C>T rs79635160 0.00123
NM_030973.4(MED25):c.354C>T (p.Leu118=) rs145574885 0.00110
NM_030973.4(MED25):c.664C>T (p.Leu222=) rs147538736 0.00046
NM_030973.4(MED25):c.135-6T>G rs199743509 0.00036
NM_030973.4(MED25):c.1572C>T (p.Gly524=) rs559482732 0.00005
NM_030973.4(MED25):c.1210G>A (p.Gly404Arg) rs1213960931 0.00001
NM_030973.4(MED25):c.275A>T (p.Tyr92Phe) rs549136898 0.00001
NM_030973.4(MED25):c.395G>A (p.Arg132His) rs1441155267 0.00001
NM_030973.4(MED25):c.526-16G>A rs756139455 0.00001
NM_030973.4(MED25):c.1128G>C (p.Val376=) rs763665593
NM_030973.4(MED25):c.1674+19C>T rs752522
NM_030973.4(MED25):c.597C>A (p.Ala199=) rs149788020
NM_030973.4(MED25):c.597C>T (p.Ala199=) rs149788020

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