ClinVar Miner

List of variants in gene TRPM4 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_017636.4(TRPM4):c.3641-19C>G rs7256050 0.01753
NM_017636.4(TRPM4):c.127G>A (p.Ala43Thr) rs112149155 0.00028
NM_017636.4(TRPM4):c.1409A>G (p.Asn470Ser) rs746075675 0.00019
NM_017636.4(TRPM4):c.2774A>C (p.Lys925Thr) rs752778561 0.00019
NM_017636.4(TRPM4):c.2535C>G (p.Pro845=) rs560849729 0.00015
NM_017636.4(TRPM4):c.857C>T (p.Thr286Met) rs775793134 0.00015
NM_017636.4(TRPM4):c.754C>T (p.Arg252Cys) rs771728837 0.00014
NM_017636.4(TRPM4):c.1139C>T (p.Ala380Val) rs150894548 0.00011
NM_017636.4(TRPM4):c.338G>A (p.Arg113His) rs149335121 0.00011
NM_017636.4(TRPM4):c.1324C>T (p.Arg442Cys) rs148867331 0.00010
NM_017636.4(TRPM4):c.2953+5G>C rs200998908 0.00010
NM_017636.4(TRPM4):c.1756G>C (p.Val586Leu) rs369462197 0.00009
NM_017636.4(TRPM4):c.2638G>A (p.Gly880Ser) rs762428211 0.00008
NM_017636.4(TRPM4):c.286C>T (p.Arg96Ter) rs148855956 0.00008
NM_017636.4(TRPM4):c.1050G>A (p.Gln350=) rs542569450 0.00007
NM_017636.4(TRPM4):c.2116C>T (p.Arg706Cys) rs199552085 0.00007
NM_017636.4(TRPM4):c.2840C>A (p.Ala947Asp) rs368175948 0.00007
NM_017636.4(TRPM4):c.416G>A (p.Arg139His) rs200360191 0.00007
NM_017636.4(TRPM4):c.1817C>G (p.Ala606Gly) rs771088249 0.00006
NM_017636.4(TRPM4):c.2732C>T (p.Thr911Met) rs148006852 0.00006
NM_017636.4(TRPM4):c.1495C>T (p.Arg499Trp) rs371377895 0.00005
NM_017636.4(TRPM4):c.1150+1G>A rs200132598 0.00004
NM_017636.4(TRPM4):c.1308C>A (p.Asp436Glu) rs200262546 0.00004
NM_017636.4(TRPM4):c.3184C>G (p.Arg1062Gly) rs375523320 0.00004
NM_017636.4(TRPM4):c.2778+1G>A rs756554490 0.00003
NM_017636.4(TRPM4):c.345G>A (p.Pro115=) rs750991001 0.00003
NM_017636.4(TRPM4):c.3563G>T (p.Trp1188Leu) rs1064796865 0.00003
NM_017636.4(TRPM4):c.582C>A (p.Val194=) rs914389404 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.1885G>A (p.Glu629Lys) rs762104169 0.00002
NM_017636.4(TRPM4):c.2420C>T (p.Pro807Leu) rs142257045 0.00002
NM_017636.4(TRPM4):c.2733G>A (p.Thr911=) rs756464554 0.00002
NM_017636.4(TRPM4):c.2912A>G (p.Tyr971Cys) rs199577978 0.00002
NM_017636.4(TRPM4):c.2992G>A (p.Gly998Ser) rs144702920 0.00002
NM_017636.4(TRPM4):c.3043T>G (p.Tyr1015Asp) rs757067985 0.00002
NM_017636.4(TRPM4):c.749G>A (p.Arg250His) rs778711356 0.00002
NM_017636.4(TRPM4):c.865G>A (p.Glu289Lys) rs770369257 0.00002
NM_017636.4(TRPM4):c.935C>T (p.Ala312Val) rs138095759 0.00002
NM_017636.4(TRPM4):c.*316G>A rs990395031 0.00001
NM_017636.4(TRPM4):c.11C>G (p.Pro4Arg) rs1318656879 0.00001
NM_017636.4(TRPM4):c.1263+2T>G rs1005829535 0.00001
NM_017636.4(TRPM4):c.1893T>C (p.Tyr631=) rs765927799 0.00001
NM_017636.4(TRPM4):c.2205T>C (p.Pro735=) rs200681329 0.00001
NM_017636.4(TRPM4):c.2330G>A (p.Gly777Asp) rs771427749 0.00001
NM_017636.4(TRPM4):c.24G>A (p.Gln8=) rs2041543043 0.00001
NM_017636.4(TRPM4):c.2564G>T (p.Arg855Leu) rs1288174566 0.00001
NM_017636.4(TRPM4):c.2738A>G (p.Asn913Ser) rs749667228 0.00001
NM_017636.4(TRPM4):c.2895C>T (p.Arg965=) rs1271791433 0.00001
NM_017636.4(TRPM4):c.2904C>G (p.Tyr968Ter) rs1179368021 0.00001
NM_017636.4(TRPM4):c.2981C>T (p.Ser994Leu) rs575737661 0.00001
NM_017636.4(TRPM4):c.3062T>A (p.Val1021Glu) rs779059936 0.00001
NM_017636.4(TRPM4):c.3130A>T (p.Ser1044Cys) rs780227965 0.00001
NM_017636.4(TRPM4):c.3449G>T (p.Arg1150Leu) rs1273337644 0.00001
NM_017636.4(TRPM4):c.434C>T (p.Ala145Val) rs767015629 0.00001
NM_017636.4(TRPM4):c.634C>T (p.Arg212Trp) rs759593186 0.00001
NM_017636.4(TRPM4):c.635G>A (p.Arg212Gln) rs183306159 0.00001
NM_017636.4(TRPM4):c.650C>T (p.Pro217Leu) rs750644014 0.00001
NM_017636.4(TRPM4):c.712G>A (p.Gly238Ser) rs923280649 0.00001
NM_017636.4(TRPM4):c.735C>T (p.Gly245=) rs555320255 0.00001
NM_017636.4(TRPM4):c.858G>A (p.Thr286=) rs760622386 0.00001
NM_017636.4(TRPM4):c.994C>T (p.Arg332Ter) rs753753488 0.00001
NM_017636.4(TRPM4):c.1212C>A (p.Asn404Lys) rs755499876
NM_017636.4(TRPM4):c.1249del (p.Asp417fs) rs750295454
NM_017636.4(TRPM4):c.1532T>A (p.Leu511Gln) rs200508171
NM_017636.4(TRPM4):c.1603G>T (p.Glu535Ter) rs748187859
NM_017636.4(TRPM4):c.1993_1999del (p.Ala665fs) rs751139020
NM_017636.4(TRPM4):c.23A>T (p.Gln8Leu) rs1057522811
NM_017636.4(TRPM4):c.2513dup (p.Ser839fs) rs747536688
NM_017636.4(TRPM4):c.2645+1G>A rs1568485293
NM_017636.4(TRPM4):c.2664C>G (p.Tyr888Ter) rs2145967337
NM_017636.4(TRPM4):c.2665del (p.His889fs) rs777047595
NM_017636.4(TRPM4):c.2749G>C (p.Gly917Arg) rs745340937
NM_017636.4(TRPM4):c.2785G>A (p.Asp929Asn) rs1555762844
NM_017636.4(TRPM4):c.2894G>A (p.Arg965His) rs150452571
NM_017636.4(TRPM4):c.2915T>A (p.Leu972Gln) rs2145969416
NM_017636.4(TRPM4):c.2932A>G (p.Ile978Val) rs962480684
NM_017636.4(TRPM4):c.3329-8C>G rs369748756
NM_017636.4(TRPM4):c.3339_3342del (p.Ser1114fs) rs1054561100
NM_017636.4(TRPM4):c.3550C>T (p.Arg1184Cys) rs779436318
NM_017636.4(TRPM4):c.3607G>A (p.Gly1203Arg) rs916697392
NM_017636.4(TRPM4):c.678C>G (p.Asp226Glu) rs730880236
NM_017636.4(TRPM4):c.845AGA[1] (p.Lys283del) rs988711796

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