ClinVar Miner

List of variants in gene TRPM4 reported as benign by Ambry Genetics

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.2380C>T (p.Leu794=) rs3745301 0.07523
NM_017636.4(TRPM4):c.375G>A (p.Ser125=) rs34333830 0.05846
NM_017636.4(TRPM4):c.1041G>T (p.Leu347=) rs61732831 0.03220
NM_017636.4(TRPM4):c.2982G>A (p.Ser994=) rs1175810 0.03027
NM_017636.4(TRPM4):c.3024G>A (p.Ala1008=) rs35145363 0.02710
NM_017636.4(TRPM4):c.2934T>C (p.Ile978=) rs35516880 0.02629
NM_017636.4(TRPM4):c.783G>A (p.Lys261=) rs111930830 0.01836
NM_017636.4(TRPM4):c.3082C>T (p.Leu1028=) rs79286201 0.01125
NM_017636.4(TRPM4):c.322C>T (p.Arg108Cys) rs115335683 0.01074
NM_017636.4(TRPM4):c.2619C>T (p.Thr873=) rs144544237 0.00790
NM_017636.4(TRPM4):c.301G>A (p.Ala101Thr) rs113984787 0.00662
NM_017636.4(TRPM4):c.306T>G (p.Val102=) rs111783027 0.00662
NM_017636.4(TRPM4):c.755G>A (p.Arg252His) rs146564314 0.00453
NM_017636.4(TRPM4):c.3405A>C (p.Ala1135=) rs144647383 0.00450
NM_017636.4(TRPM4):c.618G>A (p.Ser206=) rs142788545 0.00422
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala) rs56355369 0.00373
NM_017636.4(TRPM4):c.3611C>T (p.Pro1204Leu) rs150391806 0.00310
NM_017636.4(TRPM4):c.3427A>G (p.Ser1143Gly) rs138603244 0.00198
NM_017636.4(TRPM4):c.2209G>A (p.Gly737Arg) rs145847114 0.00165
NM_017636.4(TRPM4):c.1459_1494del (p.Lys487_Leu498del) rs878855029
NM_017636.4(TRPM4):c.2283_2294del (p.759_762CGGR[1]) rs113100797
NM_017636.4(TRPM4):c.243G>A (p.Thr81=) rs375928899

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