ClinVar Miner

List of variants in gene TMEM127 reported as uncertain significance for adrenal gland pheochromocytoma

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_017849.3(TMEM127):c.*1178A>G rs748572058
NM_017849.3(TMEM127):c.*1197T>C rs886056442
NM_017849.3(TMEM127):c.*1252C>G rs886056441
NM_017849.3(TMEM127):c.*1620C>T rs886056440
NM_017849.3(TMEM127):c.*1638G>C rs753339060
NM_017849.3(TMEM127):c.*1819C>A rs551671260
NM_017849.3(TMEM127):c.*1849T>G rs867431947
NM_017849.3(TMEM127):c.*1883_*1886dupTCTG rs886056439
NM_017849.3(TMEM127):c.*2121G>T rs778493549
NM_017849.3(TMEM127):c.*2245A>G rs886056438
NM_017849.3(TMEM127):c.*2270dupT rs886056437
NM_017849.3(TMEM127):c.*2291_*2292delAA rs566328757
NM_017849.3(TMEM127):c.*2445G>T rs886056436
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.*2760A>C rs886056431
NM_017849.3(TMEM127):c.*2845T>G rs182729595
NM_017849.3(TMEM127):c.*3025G>C rs886056430
NM_017849.3(TMEM127):c.*3348G>C rs886056429
NM_017849.3(TMEM127):c.*3560G>T rs886056428
NM_017849.3(TMEM127):c.*3568C>G rs886056427
NM_017849.3(TMEM127):c.*662G>A rs886056445
NM_017849.3(TMEM127):c.*760dupA rs371530522
NM_017849.3(TMEM127):c.*883C>G rs886056443
NM_017849.3(TMEM127):c.-131-7C>T rs886056450
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.182G>C (p.Cys61Ser) rs886056448
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.427G>A (p.Val143Ile) rs772153618
NM_017849.3(TMEM127):c.472C>G (p.Gln158Glu) rs769988721
NM_017849.3(TMEM127):c.589C>T (p.Arg197Cys) rs140860906
NM_017849.3(TMEM127):c.654G>A (p.Glu218=) rs776822044

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