ClinVar Miner

List of variants in gene GRIN2A 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: 80
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HGVS dbSNP
NM_000833.5(GRIN2A):c.*1058T>A rs886052546
NM_000833.5(GRIN2A):c.*1432del rs569463295
NM_000833.5(GRIN2A):c.*1535C>T rs886052545
NM_000833.5(GRIN2A):c.*1539T>G rs886052544
NM_000833.5(GRIN2A):c.*1806G>A rs886052543
NM_000833.5(GRIN2A):c.*1998A>T rs886052542
NM_000833.5(GRIN2A):c.*2053C>T rs775312419
NM_000833.5(GRIN2A):c.*2556C>T rs886052541
NM_000833.5(GRIN2A):c.*2622A>T rs886052540
NM_000833.5(GRIN2A):c.*268G>A rs886052553
NM_000833.5(GRIN2A):c.*2771_*2774dup rs35189803
NM_000833.5(GRIN2A):c.*2773_*2774dup rs35189803
NM_000833.5(GRIN2A):c.*2775_*2776insA rs886052539
NM_000833.5(GRIN2A):c.*2835C>T rs886052538
NM_000833.5(GRIN2A):c.*286A>G rs886052552
NM_000833.5(GRIN2A):c.*3166C>T rs886052537
NM_000833.5(GRIN2A):c.*3396T>G rs886052536
NM_000833.5(GRIN2A):c.*3543G>C rs886052535
NM_000833.5(GRIN2A):c.*3589G>A rs763658518
NM_000833.5(GRIN2A):c.*4207G>A rs747470370
NM_000833.5(GRIN2A):c.*5006G>A rs773012536
NM_000833.5(GRIN2A):c.*5109G>C rs886052534
NM_000833.5(GRIN2A):c.*5161C>T rs369083217
NM_000833.5(GRIN2A):c.*542_*544del rs760275969
NM_000833.5(GRIN2A):c.*545G>C rs886052551
NM_000833.5(GRIN2A):c.*5471T>C rs886052533
NM_000833.5(GRIN2A):c.*5473G>A rs886052532
NM_000833.5(GRIN2A):c.*574C>A rs886052550
NM_000833.5(GRIN2A):c.*5775dup rs202247656
NM_000833.5(GRIN2A):c.*5790del rs74985384
NM_000833.5(GRIN2A):c.*6042A>C rs780823999
NM_000833.5(GRIN2A):c.*6178T>C rs886052531
NM_000833.5(GRIN2A):c.*650C>G rs886052549
NM_000833.5(GRIN2A):c.*6599T>C rs886052530
NM_000833.5(GRIN2A):c.*6659G>A rs886052529
NM_000833.5(GRIN2A):c.*6760G>A rs886052528
NM_000833.5(GRIN2A):c.*678G>A rs886052548
NM_000833.5(GRIN2A):c.*6897del rs886052527
NM_000833.5(GRIN2A):c.*7009_*7010CA[9] rs113553391
NM_000833.5(GRIN2A):c.*7112A>C rs143274147
NM_000833.5(GRIN2A):c.*7207G>A rs886052525
NM_000833.5(GRIN2A):c.*7278G>T rs886052524
NM_000833.5(GRIN2A):c.*7293del rs58903398
NM_000833.5(GRIN2A):c.*7379A>G rs886052522
NM_000833.5(GRIN2A):c.*7483C>T rs551009533
NM_000833.5(GRIN2A):c.*7775C>T rs886052521
NM_000833.5(GRIN2A):c.*7897C>T rs886052520
NM_000833.5(GRIN2A):c.*8156A>G rs886052519
NM_000833.5(GRIN2A):c.*8359T>C rs886052518
NM_000833.5(GRIN2A):c.*8398G>A rs886052517
NM_000833.5(GRIN2A):c.*8542T>C rs886052516
NM_000833.5(GRIN2A):c.*8609C>T rs760313721
NM_000833.5(GRIN2A):c.*8626G>C rs886052515
NM_000833.5(GRIN2A):c.*8781G>A rs886052514
NM_000833.5(GRIN2A):c.*9207G>A rs886052513
NM_000833.5(GRIN2A):c.*971C>A rs886052547
NM_000833.5(GRIN2A):c.-34C>G rs564039694
NM_000833.5(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009
NM_000833.5(GRIN2A):c.1263C>T (p.Asp421=) rs781215527
NM_000833.5(GRIN2A):c.1317C>G (p.Phe439Leu) rs752012396
NM_000833.5(GRIN2A):c.1498-14_1498-13del rs1491547779
NM_000833.5(GRIN2A):c.2497A>G (p.Ile833Val) rs774656858
NM_000833.5(GRIN2A):c.3138A>G (p.Leu1046=) rs773244936
NM_000833.5(GRIN2A):c.3561C>T (p.Tyr1187=) rs750802726
NM_000833.5(GRIN2A):c.3668C>G (p.Thr1223Ser) rs770966136
NM_000833.5(GRIN2A):c.3678C>T (p.Gly1226=) rs749144109
NM_000833.5(GRIN2A):c.3809A>T (p.Asp1270Val) rs750649530
NM_000833.5(GRIN2A):c.3993C>A (p.Val1331=) rs886052554
NM_000833.5(GRIN2A):c.568A>G (p.Thr190Ala) rs886051634
NM_000833.5(GRIN2A):c.747C>T (p.Thr249=) rs774169125
NM_001134407.3(GRIN2A):c.*2509G>A rs530124672
NM_001134407.3(GRIN2A):c.*2544C>T rs766920527
NM_001134407.3(GRIN2A):c.*7289T>A rs868376839
NM_001134407.3(GRIN2A):c.*7982A>C rs766455387
NM_001134407.3(GRIN2A):c.1119A>G (p.Glu373=) rs368406915
NM_001134407.3(GRIN2A):c.1380C>T (p.Cys460=) rs375291296
NM_001134407.3(GRIN2A):c.2007+10C>T rs368110989
NM_001134407.3(GRIN2A):c.2532G>A (p.Lys844=) rs754414929
NM_001134407.3(GRIN2A):c.4353A>T (p.Arg1451Ser) rs143693526
NM_001134407.3(GRIN2A):c.979C>G (p.Pro327Ala) rs771168389

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