ClinVar Miner

List of variants in gene TRPM4 reported as benign for cardiac rhythm disease

Included ClinVar conditions (118):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.2019+25C>G rs1175791 0.34480
NM_017636.4(TRPM4):c.-12G>A rs3760663 0.20754
NM_017636.4(TRPM4):c.92+31A>G rs11882563 0.19699
NM_017636.4(TRPM4):c.268-23G>A rs68004247 0.14813
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.2210+11C>G rs1175796 0.05613
NM_017636.4(TRPM4):c.1151-20T>A rs11668638 0.04248
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.1050+13_1050+16dup rs137898843 0.02485
NM_017636.4(TRPM4):c.267+14C>G rs113040724 0.02235
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.3641-19C>G rs7256050 0.01753
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.448+6C>T rs78051297 0.01005
NM_017636.4(TRPM4):c.2953+15G>A rs115274216 0.00850
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.870C>T (p.Asn290=) rs141997826 0.00389
NM_017636.4(TRPM4):c.1682A>C (p.Asp561Ala) rs56355369 0.00373
NM_017636.4(TRPM4):c.449-14C>T rs112328642 0.00356
NM_017636.4(TRPM4):c.3611C>T (p.Pro1204Leu) rs150391806 0.00310
NM_017636.4(TRPM4):c.1368C>G (p.Thr456=) rs56118173 0.00274
NM_017636.4(TRPM4):c.93-18C>T rs150300993 0.00260
NM_017636.4(TRPM4):c.3427A>G (p.Ser1143Gly) rs138603244 0.00198
NM_017636.4(TRPM4):c.1575G>A (p.Trp525Ter) rs71352737 0.00168
NM_017636.4(TRPM4):c.2209G>A (p.Gly737Arg) rs145847114 0.00165
NM_017636.4(TRPM4):c.1873+13C>G rs184297107 0.00154
NM_017636.4(TRPM4):c.1164G>A (p.Ser388=) rs144201184 0.00095
NM_017636.4(TRPM4):c.3641-17T>G rs369065473 0.00053
NM_017636.4(TRPM4):c.2674C>T (p.Arg892Cys) rs147854826 0.00047
NM_017636.4(TRPM4):c.342C>G (p.Ala114=) rs144434701 0.00045
NM_017636.4(TRPM4):c.2254C>T (p.Gln752Ter) rs769917929 0.00041
NM_017636.4(TRPM4):c.2645+16C>A rs367554662 0.00021
NM_017636.4(TRPM4):c.2535C>G (p.Pro845=) rs560849729 0.00015
NM_017636.4(TRPM4):c.1051-9A>G rs200985127 0.00013
NM_017636.4(TRPM4):c.2954-11T>C rs774806552 0.00011
NM_017636.4(TRPM4):c.1150+15C>G rs368936434 0.00010
NM_017636.4(TRPM4):c.2779-15C>G rs148833212 0.00006
NM_017636.4(TRPM4):c.2712G>T (p.Val904=) rs143447932 0.00005
NM_017636.4(TRPM4):c.657C>T (p.Asp219=) rs373953725 0.00005
NM_017636.4(TRPM4):c.936G>A (p.Ala312=) rs577738761 0.00004
NM_017636.4(TRPM4):c.1442C>G (p.Ser481Cys) rs200246268 0.00002
NM_017636.4(TRPM4):c.168C>T (p.Ala56=) rs371192886 0.00001
NM_017636.4(TRPM4):c.354G>C (p.Val118=) rs566463803 0.00001
NM_017636.4(TRPM4):c.613-5C>T rs747796161 0.00001
NM_017636.4(TRPM4):c.92+11C>A rs142317684 0.00001
NM_017636.4(TRPM4):c.1459_1494del (p.Lys487_Leu498del) rs878855029
NM_017636.4(TRPM4):c.1608+25dup
NM_017636.4(TRPM4):c.1609-16del
NM_017636.4(TRPM4):c.1843C>T (p.Leu615=) rs532994978
NM_017636.4(TRPM4):c.2020-5dup
NM_017636.4(TRPM4):c.2283_2294del (p.759_762CGGR[1]) rs113100797
NM_017636.4(TRPM4):c.243G>A (p.Thr81=) rs375928899
NM_017636.4(TRPM4):c.249C>T (p.Ala83=) rs142270489
NM_017636.4(TRPM4):c.2646-17A>T rs116370720
NM_017636.4(TRPM4):c.3131+17C>T rs201977777
NM_017636.4(TRPM4):c.479C>T (p.Thr160Met)
NM_017636.4(TRPM4):c.858+9del
NM_017636.4(TRPM4):c.92+12G>A rs377431946

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