ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_000314.7(PTEN):c.*1034T>G rs886047412
NM_000314.7(PTEN):c.*1119A>T rs376153776
NM_000314.7(PTEN):c.*1150C>A rs886047414
NM_000314.7(PTEN):c.*1173G>A rs886047415
NM_000314.7(PTEN):c.*1202T>C rs886047416
NM_000314.7(PTEN):c.*124C>T rs886047399
NM_000314.7(PTEN):c.*1363dup rs886047417
NM_000314.7(PTEN):c.*1436_*1437insGTT rs563751927
NM_000314.7(PTEN):c.*1440T>G rs886047422
NM_000314.7(PTEN):c.*1442T>G rs886047423
NM_000314.7(PTEN):c.*1449T>G rs886047424
NM_000314.7(PTEN):c.*1457_*1459del rs5786797
NM_000314.7(PTEN):c.*1458_*1459del rs5786797
NM_000314.7(PTEN):c.*1459T>A rs886047425
NM_000314.7(PTEN):c.*1459del rs5786797
NM_000314.7(PTEN):c.*1459dup rs5786797
NM_000314.7(PTEN):c.*1460A>T rs35632884
NM_000314.7(PTEN):c.*1462del rs886047418
NM_000314.7(PTEN):c.*1529C>T rs886047427
NM_000314.7(PTEN):c.*1572C>T rs886047428
NM_000314.7(PTEN):c.*1576T>A rs886047429
NM_000314.7(PTEN):c.*1583G>A rs548599209
NM_000314.7(PTEN):c.*1591A>G rs886047430
NM_000314.7(PTEN):c.*1669C>A rs886047431
NM_000314.7(PTEN):c.*1762G>A rs886047432
NM_000314.7(PTEN):c.*176del rs886047400
NM_000314.7(PTEN):c.*178T>G rs886047401
NM_000314.7(PTEN):c.*2027A>C rs886047433
NM_000314.7(PTEN):c.*2061T>A rs886047434
NM_000314.7(PTEN):c.*2110G>T rs886047435
NM_000314.7(PTEN):c.*2200C>A rs886047436
NM_000314.7(PTEN):c.*2203A>G rs886047437
NM_000314.7(PTEN):c.*2263_*2265ATT[1] rs775116816
NM_000314.7(PTEN):c.*2408_*2414del rs886047439
NM_000314.7(PTEN):c.*2437A>G rs886047440
NM_000314.7(PTEN):c.*2558C>A rs886047441
NM_000314.7(PTEN):c.*2683_*2684insACA rs886047442
NM_000314.7(PTEN):c.*2685_*2687CTC[1] rs886047443
NM_000314.7(PTEN):c.*2746C>A rs886047444
NM_000314.7(PTEN):c.*2771T>C rs886047445
NM_000314.7(PTEN):c.*2789C>G rs886047446
NM_000314.7(PTEN):c.*2821A>T rs11591427
NM_000314.7(PTEN):c.*2905G>C rs886047447
NM_000314.7(PTEN):c.*3033C>A rs886047448
NM_000314.7(PTEN):c.*3083C>A rs886047449
NM_000314.7(PTEN):c.*3177A>G rs886047450
NM_000314.7(PTEN):c.*430A>G rs886047402
NM_000314.7(PTEN):c.*515T>C rs886047403
NM_000314.7(PTEN):c.*597C>A rs886047404
NM_000314.7(PTEN):c.*621G>T rs886047405
NM_000314.7(PTEN):c.*631C>A rs886047406
NM_000314.7(PTEN):c.*640C>A rs886047407
NM_000314.7(PTEN):c.*667A>T rs886047409
NM_000314.7(PTEN):c.*74T>C rs886047398
NM_000314.7(PTEN):c.*790A>G rs886047411
NM_000314.7(PTEN):c.*791_*793del rs886047410
NM_000314.7(PTEN):c.-111G>T rs761148721
NM_000314.7(PTEN):c.-121A>G rs886047395
NM_000314.7(PTEN):c.-190G>A rs886047394
NM_000314.7(PTEN):c.-246C>T rs886047393
NM_000314.7(PTEN):c.-295T>C rs886047392
NM_000314.7(PTEN):c.-32_-30CCT[1] rs749497048
NM_000314.7(PTEN):c.-355G>A rs886047391
NM_000314.7(PTEN):c.-425G>T rs886047390
NM_000314.7(PTEN):c.-458G>T rs886047389
NM_000314.7(PTEN):c.-461G>A rs886047388
NM_000314.7(PTEN):c.-506del rs886047386
NM_000314.7(PTEN):c.-734G>A rs886047384
NM_000314.7(PTEN):c.-736C>G rs886047383
NM_000314.7(PTEN):c.210-7_210-3del rs587780544
NM_000314.7(PTEN):c.802-2del rs886047397

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