ClinVar Miner

List of variants in gene TRPM4 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.-12G>A rs3760663 0.20754
NM_017636.4(TRPM4):c.449-10G>A rs78444754 0.02013
NM_017636.4(TRPM4):c.783G>A (p.Lys261=) rs111930830 0.01836
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.618G>A (p.Ser206=) rs142788545 0.00422
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala) rs56355369 0.00373
NM_017636.4(TRPM4):c.2209G>A (p.Gly737Arg) rs145847114 0.00165
NM_017636.4(TRPM4):c.988G>A (p.Glu330Lys) rs145771389 0.00118
NM_017636.4(TRPM4):c.2740A>T (p.Lys914Ter) rs140799936 0.00094
NM_017636.4(TRPM4):c.1376G>A (p.Arg459His) rs142312281 0.00086
NM_017636.4(TRPM4):c.2561A>G (p.Gln854Arg) rs172155862 0.00078
NM_017636.4(TRPM4):c.2531G>A (p.Gly844Asp) rs200038418 0.00064
NM_017636.4(TRPM4):c.2254C>T (p.Gln752Ter) rs769917929 0.00041
NM_017636.4(TRPM4):c.308A>G (p.Tyr103Cys) rs144781529 0.00041
NM_017636.4(TRPM4):c.2156G>A (p.Arg719Gln) rs78381230 0.00018
NM_017636.4(TRPM4):c.2535C>G (p.Pro845=) rs560849729 0.00015
NM_017636.4(TRPM4):c.1756G>C (p.Val586Leu) rs369462197 0.00009
NM_017636.4(TRPM4):c.2712G>T (p.Val904=) rs143447932 0.00005
NM_017636.4(TRPM4):c.1473A>G (p.Leu491=) rs142739227 0.00001
NM_017636.4(TRPM4):c.19G>A (p.Glu7Lys) rs267607142 0.00001
NM_017636.4(TRPM4):c.2231A>T (p.Lys744Met) rs569301210 0.00001
NM_017636.4(TRPM4):c.2754C>G (p.Pro918=) rs202245171 0.00001
NM_017636.4(TRPM4):c.1180C>G (p.Leu394Val)
NM_017636.4(TRPM4):c.1459_1494del (p.Lys487_Leu498del) rs878855029
NM_017636.4(TRPM4):c.1566G>A (p.Gly522=) rs1968042908
NM_017636.4(TRPM4):c.2542G>A (p.Gly848Ser)
NM_017636.4(TRPM4):c.2542G>C (p.Gly848Arg)
NM_017636.4(TRPM4):c.2779-10C>A
NM_017636.4(TRPM4):c.2953+7G>A
NM_017636.4(TRPM4):c.3219C>T (p.Pro1073=)
NM_017636.4(TRPM4):c.601A>G (p.Ile201Val)
NM_017636.4(TRPM4):c.708C>T (p.Asp236=)
NM_017636.4(TRPM4):c.846G>A (p.Glu282=)

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