ClinVar Miner

List of variants in gene TMEM127 reported as likely benign for adrenal gland pheochromocytoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP
NM_017849.3(TMEM127):c.*1163C>T rs11691019
NM_017849.3(TMEM127):c.*1233C>T rs536712285
NM_017849.3(TMEM127):c.*1306C>T rs148119945
NM_017849.3(TMEM127):c.*1406G>A rs534881507
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>G rs551671260
NM_017849.3(TMEM127):c.*2012C>T rs149122699
NM_017849.3(TMEM127):c.*2086C>T rs13418193
NM_017849.3(TMEM127):c.*2101_*2103delTTT rs3832113
NM_017849.3(TMEM127):c.*2171C>T rs555968113
NM_017849.3(TMEM127):c.*2300G>A rs117655540
NM_017849.3(TMEM127):c.*2498C>T rs191565203
NM_017849.3(TMEM127):c.*2719G>A rs140164805
NM_017849.3(TMEM127):c.*2888delT rs139762991
NM_017849.3(TMEM127):c.*2966C>G rs17119378
NM_017849.3(TMEM127):c.*3134C>T rs566067694
NM_017849.3(TMEM127):c.*3206_*3208delGTT rs141956691
NM_017849.3(TMEM127):c.*3209A>G rs186348610
NM_017849.3(TMEM127):c.*338G>A rs13022177
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.*674dupC rs201871634
NM_017849.3(TMEM127):c.*760delA rs371530522
NM_017849.3(TMEM127):c.*980G>A rs77989183
NM_017849.3(TMEM127):c.-59C>T rs542087360
NM_017849.3(TMEM127):c.-87C>T rs527792197
NM_017849.3(TMEM127):c.217G>C (p.Gly73Arg) rs121908820
NM_017849.3(TMEM127):c.268G>A (p.Val90Met) rs121908823
NM_017849.3(TMEM127):c.394G>A (p.Ala132Thr) rs750870974
NM_017849.3(TMEM127):c.409+7C>T rs189327749
NM_017849.3(TMEM127):c.53C>T (p.Pro18Leu) rs377740271
NM_017849.3(TMEM127):c.565C>T (p.Leu189=) rs146965678

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