ClinVar Miner

List of variants in gene TMEM127 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_017849.4(TMEM127):c.*2291_*2292del rs566328757 0.00091
NM_017849.4(TMEM127):c.*2128C>A rs533813582 0.00061
NM_017849.4(TMEM127):c.*980G>A rs77989183 0.00056
NM_017849.4(TMEM127):c.*1849T>G rs867431947 0.00046
NM_017849.4(TMEM127):c.*612C>T rs549115489 0.00024
NM_017849.4(TMEM127):c.*3396G>A rs762419401 0.00020
NM_017849.4(TMEM127):c.*1257C>G rs574710319 0.00018
NM_017849.4(TMEM127):c.*2719G>A rs140164805 0.00014
NM_017849.4(TMEM127):c.*1178A>G rs748572058 0.00012
NM_017849.4(TMEM127):c.*1638G>C rs753339060 0.00009
NM_017849.4(TMEM127):c.*3134C>T rs566067694 0.00009
NM_017849.4(TMEM127):c.*3025G>C rs886056430 0.00008
NM_017849.4(TMEM127):c.*2121G>T rs778493549 0.00006
NM_017849.4(TMEM127):c.*2875A>G rs915390483 0.00006
NM_017849.4(TMEM127):c.*3560G>T rs886056428 0.00006
NM_017849.4(TMEM127):c.*1879G>A rs766485637 0.00005
NM_017849.4(TMEM127):c.*2800T>G rs1037492575 0.00005
NM_017849.4(TMEM127):c.*3271A>G rs569110562 0.00005
NM_017849.4(TMEM127):c.-220T>C rs886056452 0.00005
NM_017849.4(TMEM127):c.*16C>G rs1251288941 0.00004
NM_017849.4(TMEM127):c.*3049T>C rs1242736942 0.00004
NM_017849.4(TMEM127):c.*2503C>T rs886056435 0.00003
NM_017849.4(TMEM127):c.*2563G>A rs1483429634 0.00003
NM_017849.4(TMEM127):c.-242G>A rs886056453 0.00003
NM_017849.4(TMEM127):c.379C>T (p.Arg127Cys) rs746883021 0.00003
NM_017849.4(TMEM127):c.*1620C>T rs886056440 0.00002
NM_017849.4(TMEM127):c.*2171C>T rs555968113 0.00002
NM_017849.4(TMEM127):c.*1784C>T rs571939749 0.00001
NM_017849.4(TMEM127):c.*179C>T rs932134479 0.00001
NM_017849.4(TMEM127):c.*1822T>C rs144880727 0.00001
NM_017849.4(TMEM127):c.*2245A>G rs886056438 0.00001
NM_017849.4(TMEM127):c.*2299C>T rs896902158 0.00001
NM_017849.4(TMEM127):c.*2445G>T rs886056436 0.00001
NM_017849.4(TMEM127):c.*2518C>A rs1181236784 0.00001
NM_017849.4(TMEM127):c.*2760A>C rs886056431 0.00001
NM_017849.4(TMEM127):c.*2911C>T rs1461511429 0.00001
NM_017849.4(TMEM127):c.*3391G>A rs1260000636 0.00001
NM_017849.4(TMEM127):c.*340G>A rs1032246352 0.00001
NM_017849.4(TMEM127):c.*3568C>G rs886056427 0.00001
NM_017849.4(TMEM127):c.-196C>T rs886056451 0.00001
NM_017849.4(TMEM127):c.299G>C (p.Cys100Ser) rs886056447 0.00001
NM_017849.4(TMEM127):c.*1197T>C rs886056442
NM_017849.4(TMEM127):c.*1252C>G rs886056441
NM_017849.4(TMEM127):c.*1406G>A rs534881507
NM_017849.4(TMEM127):c.*1819C>A rs551671260
NM_017849.4(TMEM127):c.*1819C>G rs551671260
NM_017849.4(TMEM127):c.*1883_*1886dup rs886056439
NM_017849.4(TMEM127):c.*2270dup rs886056437
NM_017849.4(TMEM127):c.*2411C>A rs1158489118
NM_017849.4(TMEM127):c.*249G>A rs886056446
NM_017849.4(TMEM127):c.*2548T>C rs886056434
NM_017849.4(TMEM127):c.*2642C>T rs886056433
NM_017849.4(TMEM127):c.*2684C>G rs1684078512
NM_017849.4(TMEM127):c.*2717C>G rs886056432
NM_017849.4(TMEM127):c.*2860A>G rs1289173127
NM_017849.4(TMEM127):c.*3348G>C rs886056429
NM_017849.4(TMEM127):c.*662G>A rs886056445
NM_017849.4(TMEM127):c.*760dup rs371530522
NM_017849.4(TMEM127):c.*866C>T rs926874804
NM_017849.4(TMEM127):c.*883C>G rs886056443
NM_017849.4(TMEM127):c.*980G>C rs77989183
NM_017849.4(TMEM127):c.144C>T (p.Leu48=) rs1684391372
NM_017849.4(TMEM127):c.182G>C (p.Cys61Ser) rs886056448
NM_017849.4(TMEM127):c.253A>C (p.Met85Leu) rs771261665
NM_017849.4(TMEM127):c.472C>G (p.Gln158Glu) rs769988721

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