ClinVar Miner

List of variants in gene TMEM127 studied for cardiovascular organ benign neoplasm

Included ClinVar conditions (45):
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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP
NM_001193304.3(TMEM127):c.*3200_*3202GTT[2] rs141956691
NM_001193304.3(TMEM127):c.117_120del (p.Ile41fs) rs121908816
NM_001193304.3(TMEM127):c.217G>C (p.Gly73Arg) rs121908820
NM_001193304.3(TMEM127):c.268G>A (p.Val90Met) rs121908823
NM_017849.3(TMEM127):c.*1163C>T rs11691019
NM_017849.3(TMEM127):c.*1178A>G rs748572058
NM_017849.3(TMEM127):c.*1197T>C rs886056442
NM_017849.3(TMEM127):c.*1233C>T rs536712285
NM_017849.3(TMEM127):c.*1252C>G rs886056441
NM_017849.3(TMEM127):c.*1301T>C rs3770239
NM_017849.3(TMEM127):c.*1306C>T rs148119945
NM_017849.3(TMEM127):c.*1406G>A rs534881507
NM_017849.3(TMEM127):c.*1620C>T rs886056440
NM_017849.3(TMEM127):c.*1638G>C rs753339060
NM_017849.3(TMEM127):c.*1723C>T rs551200730
NM_017849.3(TMEM127):c.*1772G>A rs537225254
NM_017849.3(TMEM127):c.*1784C>T rs571939749
NM_017849.3(TMEM127):c.*1819C>A rs551671260
NM_017849.3(TMEM127):c.*1819C>G rs551671260
NM_017849.3(TMEM127):c.*1849T>G rs867431947
NM_017849.3(TMEM127):c.*1883_*1886dup rs886056439
NM_017849.3(TMEM127):c.*1958A>C rs7058
NM_017849.3(TMEM127):c.*2012C>T rs149122699
NM_017849.3(TMEM127):c.*2086C>T rs13418193
NM_017849.3(TMEM127):c.*2101_*2103del rs3832113
NM_017849.3(TMEM127):c.*2121G>T rs778493549
NM_017849.3(TMEM127):c.*2171C>T rs555968113
NM_017849.3(TMEM127):c.*2245A>G rs886056438
NM_017849.3(TMEM127):c.*2270dup rs886056437
NM_017849.3(TMEM127):c.*2291_*2292del rs566328757
NM_017849.3(TMEM127):c.*2300G>A rs117655540
NM_017849.3(TMEM127):c.*2445G>T rs886056436
NM_017849.3(TMEM127):c.*2498C>T rs191565203
NM_017849.3(TMEM127):c.*249G>A rs886056446
NM_017849.3(TMEM127):c.*2503C>T rs886056435
NM_017849.3(TMEM127):c.*2548T>C rs886056434
NM_017849.3(TMEM127):c.*2642C>T rs886056433
NM_017849.3(TMEM127):c.*2717C>G rs886056432
NM_017849.3(TMEM127):c.*2719G>A rs140164805
NM_017849.3(TMEM127):c.*2760A>C rs886056431
NM_017849.3(TMEM127):c.*2845T>G rs182729595
NM_017849.3(TMEM127):c.*2888del rs139762991
NM_017849.3(TMEM127):c.*2966C>G rs17119378
NM_017849.3(TMEM127):c.*3025G>C rs886056430
NM_017849.3(TMEM127):c.*3134C>T rs566067694
NM_017849.3(TMEM127):c.*3209A>G rs186348610
NM_017849.3(TMEM127):c.*3348G>C rs886056429
NM_017849.3(TMEM127):c.*338G>A rs13022177
NM_017849.3(TMEM127):c.*3560G>T rs886056428
NM_017849.3(TMEM127):c.*3568C>G rs886056427
NM_017849.3(TMEM127):c.*3569C>T rs140274612
NM_017849.3(TMEM127):c.*502C>T rs191970829
NM_017849.3(TMEM127):c.*50C>T rs72937654
NM_017849.3(TMEM127):c.*57C>T rs147532087
NM_017849.3(TMEM127):c.*662G>A rs886056445
NM_017849.3(TMEM127):c.*674dup rs201871634
NM_017849.3(TMEM127):c.*760del rs371530522
NM_017849.3(TMEM127):c.*760dup rs371530522
NM_017849.3(TMEM127):c.*883C>G rs886056443
NM_017849.3(TMEM127):c.*980G>A rs77989183
NM_017849.3(TMEM127):c.-131-7C>T rs886056450
NM_017849.3(TMEM127):c.-18C>T rs121908813
NM_017849.3(TMEM127):c.-196C>T rs886056451
NM_017849.3(TMEM127):c.-220T>C rs886056452
NM_017849.3(TMEM127):c.-242G>A rs886056453
NM_017849.3(TMEM127):c.-37A>G rs886056449
NM_017849.3(TMEM127):c.-59C>T rs542087360
NM_017849.3(TMEM127):c.-87C>T rs527792197
NM_017849.3(TMEM127):c.149dup (p.Pro51fs) rs121908817
NM_017849.3(TMEM127):c.158G>C (p.Trp53Ser) rs121908818
NM_017849.3(TMEM127):c.182G>C (p.Cys61Ser) rs886056448
NM_017849.3(TMEM127):c.208G>A (p.Asp70Asn) rs121908819
NM_017849.3(TMEM127):c.245-1G>T rs121908821
NM_017849.3(TMEM127):c.265_268del (p.Thr89fs) rs121908822
NM_017849.3(TMEM127):c.280C>T (p.Arg94Trp) rs121908824
NM_017849.3(TMEM127):c.281G>A (p.Arg94Gln) rs746831347
NM_017849.3(TMEM127):c.288C>T (p.Ile96=) rs758726687
NM_017849.3(TMEM127):c.299G>C (p.Cys100Ser) rs886056447
NM_017849.3(TMEM127):c.379C>T (p.Arg127Cys) rs746883021
NM_017849.3(TMEM127):c.394G>A (p.Ala132Thr) rs750870974
NM_017849.3(TMEM127):c.3G>T (p.Met1Ile) rs121908814
NM_017849.3(TMEM127):c.409+1G>T rs121908825
NM_017849.3(TMEM127):c.409+7C>T rs189327749
NM_017849.3(TMEM127):c.410-2A>C rs121908826
NM_017849.3(TMEM127):c.418T>C (p.Cys140Arg) rs121908827
NM_017849.3(TMEM127):c.419G>A (p.Cys140Tyr) rs121908828
NM_017849.3(TMEM127):c.427G>A (p.Val143Ile) rs772153618
NM_017849.3(TMEM127):c.447G>A (p.Trp149Ter) rs121908829
NM_017849.3(TMEM127):c.472C>G (p.Gln158Glu) rs769988721
NM_017849.3(TMEM127):c.475C>T (p.Gln159Ter) rs121908830
NM_017849.3(TMEM127):c.53C>T (p.Pro18Leu) rs377740271
NM_017849.3(TMEM127):c.565C>T (p.Leu189=) rs146965678
NM_017849.3(TMEM127):c.589C>T (p.Arg197Cys) rs140860906
NM_017849.3(TMEM127):c.621G>A (p.Ala207=) rs3852673
NM_017849.3(TMEM127):c.627_640dup (p.Met214fs) rs121908831
NM_017849.3(TMEM127):c.654G>A (p.Glu218=) rs776822044
NM_017849.3(TMEM127):c.76C>T (p.Gln26Ter) rs121908815

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