ClinVar Miner

List of variants in gene TRPM4 reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 114
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.-12G>A rs3760663 0.20754
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.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.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.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_017636.3(TRPM4):c.-107G>T rs112085495 0.00258
NM_017636.4(TRPM4):c.*84C>T rs192428881 0.00206
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.988G>A (p.Glu330Lys) rs145771389 0.00118
NM_017636.4(TRPM4):c.2740A>T (p.Lys914Ter) rs140799936 0.00094
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.2674C>T (p.Arg892Cys) rs147854826 0.00047
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.1242T>C (p.Phe414=) rs200633475 0.00031
NM_017636.4(TRPM4):c.127G>A (p.Ala43Thr) rs112149155 0.00028
NM_017636.4(TRPM4):c.*81G>T rs138173650 0.00024
NM_017636.4(TRPM4):c.1836G>A (p.Arg612=) rs112589404 0.00023
NM_017636.4(TRPM4):c.748C>T (p.Arg250Cys) rs144208673 0.00021
NM_017636.4(TRPM4):c.1874-9C>T rs199805560 0.00020
NM_017636.4(TRPM4):c.742C>T (p.Arg248Cys) rs373749900 0.00014
NM_017636.4(TRPM4):c.856A>G (p.Thr286Ala) rs151205002 0.00013
NM_017636.4(TRPM4):c.2954-11T>C rs774806552 0.00011
NM_017636.4(TRPM4):c.2133-9C>G rs530013543 0.00009
NM_017636.4(TRPM4):c.*119C>T rs757446153 0.00008
NM_017636.4(TRPM4):c.*234C>T rs149217174 0.00008
NM_017636.4(TRPM4):c.2020-4A>C rs369498574 0.00008
NM_017636.4(TRPM4):c.2085C>T (p.Leu695=) rs781191851 0.00008
NM_017636.4(TRPM4):c.2638G>A (p.Gly880Ser) rs762428211 0.00008
NM_017636.4(TRPM4):c.250G>A (p.Gly84Ser) rs151258293 0.00007
NM_017636.4(TRPM4):c.2779-5C>T rs374639233 0.00007
NM_017636.4(TRPM4):c.483C>T (p.Gly161=) rs147157308 0.00007
NM_017636.4(TRPM4):c.1817C>G (p.Ala606Gly) rs771088249 0.00006
NM_017636.4(TRPM4):c.1495C>T (p.Arg499Trp) rs371377895 0.00005
NM_017636.4(TRPM4):c.1873+4C>T rs746766318 0.00005
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.3184C>G (p.Arg1062Gly) rs375523320 0.00004
NM_017636.4(TRPM4):c.721G>A (p.Gly241Ser) rs886054577 0.00004
NM_017636.4(TRPM4):c.878A>G (p.Gln293Arg) rs172147855 0.00004
NM_017636.4(TRPM4):c.*6G>A rs777589593 0.00003
NM_017636.4(TRPM4):c.1150+6A>G rs762562114 0.00003
NM_017636.4(TRPM4):c.1050+1G>A rs775091137 0.00002
NM_017636.4(TRPM4):c.1466C>T (p.Pro489Leu) rs766004189 0.00002
NM_017636.4(TRPM4):c.1514A>G (p.His505Arg) rs749621197 0.00002
NM_017636.4(TRPM4):c.1727T>C (p.Met576Thr) rs371269743 0.00002
NM_017636.4(TRPM4):c.2536G>T (p.Gly846Trp) rs772659037 0.00002
NM_017636.4(TRPM4):c.3377C>G (p.Ser1126Trp) rs567938424 0.00002
NM_017636.4(TRPM4):c.3545G>A (p.Cys1182Tyr) rs757878891 0.00002
NM_017636.4(TRPM4):c.*12G>A rs761801567 0.00001
NM_017636.4(TRPM4):c.*15C>G rs750453761 0.00001
NM_017636.4(TRPM4):c.*316G>A rs990395031 0.00001
NM_017636.4(TRPM4):c.1006A>G (p.Arg336Gly) rs748424780 0.00001
NM_017636.4(TRPM4):c.1473A>G (p.Leu491=) rs142739227 0.00001
NM_017636.4(TRPM4):c.1A>G (p.Met1Val) rs969064041 0.00001
NM_017636.4(TRPM4):c.2020-11A>T rs1371239349 0.00001
NM_017636.4(TRPM4):c.2229G>A (p.Glu743=) rs745667706 0.00001
NM_017636.4(TRPM4):c.2231A>T (p.Lys744Met) rs569301210 0.00001
NM_017636.4(TRPM4):c.2274C>G (p.Cys758Trp) rs777409336 0.00001
NM_017636.4(TRPM4):c.2275T>G (p.Cys759Gly) rs757164235 0.00001
NM_017636.4(TRPM4):c.2330G>A (p.Gly777Asp) rs771427749 0.00001
NM_017636.4(TRPM4):c.2403G>T (p.Leu801=) rs1455410186 0.00001
NM_017636.4(TRPM4):c.2564G>T (p.Arg855Leu) rs1288174566 0.00001
NM_017636.4(TRPM4):c.272T>C (p.Leu91Pro) rs145677855 0.00001
NM_017636.4(TRPM4):c.291G>A (p.Thr97=) rs886054576 0.00001
NM_017636.4(TRPM4):c.3489A>G (p.Gly1163=) rs760190293 0.00001
NM_017636.4(TRPM4):c.837T>C (p.Asp279=) rs373391017 0.00001
NM_017636.4(TRPM4):c.956_958del (p.Leu319_Ala320delinsPro) rs764918057 0.00001
NM_017636.4(TRPM4):c.*116G>C rs1969374815
NM_017636.4(TRPM4):c.*180G>A rs1969376567
NM_017636.4(TRPM4):c.136G>T (p.Ala46Ser) rs751134895
NM_017636.4(TRPM4):c.1532T>A (p.Leu511Gln) rs200508171
NM_017636.4(TRPM4):c.1843C>T (p.Leu615=) rs532994978
NM_017636.4(TRPM4):c.1908G>C (p.Val636=) rs950364050
NM_017636.4(TRPM4):c.2154A>C (p.Thr718=) rs370827464
NM_017636.4(TRPM4):c.2358C>T (p.Asn786=) rs886054579
NM_017636.4(TRPM4):c.243G>A (p.Thr81=) rs375928899
NM_017636.4(TRPM4):c.2474T>C (p.Leu825Pro) rs1968659826
NM_017636.4(TRPM4):c.251G>T (p.Gly84Val) rs886054575
NM_017636.4(TRPM4):c.2529G>C (p.Gly843=) rs754769591
NM_017636.4(TRPM4):c.2645+1G>A rs1568485293
NM_017636.4(TRPM4):c.2665del (p.His889fs) rs777047595
NM_017636.4(TRPM4):c.2760C>G (p.Ile920Met) rs1968871960
NM_017636.4(TRPM4):c.2790G>A (p.Val930=) rs886054580
NM_017636.4(TRPM4):c.2835C>T (p.Gly945=) rs1600515282
NM_017636.4(TRPM4):c.3328+1G>A rs756981657
NM_017636.4(TRPM4):c.3366A>G (p.Leu1122=) rs1387528488
NM_017636.4(TRPM4):c.344del (p.Pro115fs) rs777609699
NM_017636.4(TRPM4):c.92+12G>A rs377431946

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.