ClinVar Miner

List of variants in gene TRPM4 reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
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.1682A>C (p.Asp561Ala) rs56355369 0.00373
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.2561A>G (p.Gln854Arg) rs172155862 0.00078
NM_017636.4(TRPM4):c.3641-17T>G rs369065473 0.00053
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.3329-14G>C rs777092081 0.00014
NM_017636.4(TRPM4):c.796+16C>G rs779490161 0.00014
NM_017636.4(TRPM4):c.3073G>A (p.Val1025Ile) rs186822052 0.00012
NM_017636.4(TRPM4):c.2133-9C>G rs530013543 0.00009
NM_017636.4(TRPM4):c.2779-5C>T rs374639233 0.00007
NM_017636.4(TRPM4):c.1873+4C>T rs746766318 0.00005
NM_017636.4(TRPM4):c.24+7G>A rs960522960 0.00005
NM_017636.4(TRPM4):c.268-19C>T rs377765533 0.00005
NM_017636.4(TRPM4):c.2020-8C>T rs200820404 0.00004
NM_017636.4(TRPM4):c.240C>T (p.Phe80=) rs563344549 0.00004
NM_017636.4(TRPM4):c.3012T>C (p.Pro1004=) rs76139110 0.00004
NM_017636.4(TRPM4):c.12G>A (p.Pro4=) rs1403043676 0.00003
NM_017636.4(TRPM4):c.2208C>T (p.Val736=) rs139307985 0.00003
NM_017636.4(TRPM4):c.3315C>A (p.Ala1105=) rs982072766 0.00003
NM_017636.4(TRPM4):c.92+12G>C rs377431946 0.00003
NM_017636.4(TRPM4):c.1215C>T (p.Arg405=) rs140069078 0.00001
NM_017636.4(TRPM4):c.168C>T (p.Ala56=) rs371192886 0.00001
NM_017636.4(TRPM4):c.1803C>G (p.Arg601=) rs528980972 0.00001
NM_017636.4(TRPM4):c.216C>T (p.Thr72=) rs767155832 0.00001
NM_017636.4(TRPM4):c.651G>A (p.Pro217=) rs758473371 0.00001
NM_017636.4(TRPM4):c.984A>G (p.Gln328=) rs752367612 0.00001
NM_017636.4(TRPM4):c.1332C>T (p.Leu444=) rs1229281209
NM_017636.4(TRPM4):c.1356C>T (p.Gly452=)
NM_017636.4(TRPM4):c.1971G>A (p.Leu657=) rs1555757521
NM_017636.4(TRPM4):c.2283_2294del (p.759_762CGGR[1]) rs113100797
NM_017636.4(TRPM4):c.3132-20T>C
NM_017636.4(TRPM4):c.3315C>T (p.Ala1105=) rs982072766
NM_017636.4(TRPM4):c.3329-4G>A rs374808636
NM_017636.4(TRPM4):c.3513C>T (p.Arg1171=) rs1379017824
NM_017636.4(TRPM4):c.829C>T (p.Leu277=) rs1555752825
NM_017636.4(TRPM4):c.92+12G>A rs377431946

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