ClinVar Miner

List of variants in gene GRIN2A reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.-19+36G>A rs2302711 0.65540
NM_001134407.3(GRIN2A):c.1329-105A>C rs6497540 0.39397
NM_001134407.3(GRIN2A):c.1123-177T>C rs8054791 0.38914
NM_001134407.3(GRIN2A):c.2595+152C>A rs11866328 0.38731
NM_001134407.3(GRIN2A):c.2357-247C>A rs2872825 0.38195
NM_001134407.3(GRIN2A):c.1328+181C>A rs9934477 0.34524
NM_001134407.3(GRIN2A):c.415-38487T>C rs3859123 0.33729
NM_001134407.3(GRIN2A):c.1122+320G>A rs9931155 0.33541
NM_001134407.3(GRIN2A):c.2007+101C>T rs11642764 0.28631
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193 0.27838
NM_001134407.3(GRIN2A):c.415-309G>A rs11648171 0.21984
NM_001134407.3(GRIN2A):c.415-38662C>T rs4254328 0.11675
NM_001134407.3(GRIN2A):c.1328+142A>T rs56155349 0.07739
NM_001134407.3(GRIN2A):c.1329-317del rs55939593 0.05641
NM_001134407.3(GRIN2A):c.1329-272A>G rs7200793 0.04773
NM_001134407.3(GRIN2A):c.415-63607G>T rs9934830 0.02804
NM_001134407.3(GRIN2A):c.2357-245A>C rs74008811 0.02533
NM_001134407.3(GRIN2A):c.-18-345C>A rs74006799 0.02369
NM_001134407.3(GRIN2A):c.1122+133T>C rs16966605 0.02198
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290 0.01998
NM_001134407.3(GRIN2A):c.1329-145G>C rs7194922 0.01953
NM_001134407.3(GRIN2A):c.*121G>T rs75272984 0.01949
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382 0.00763
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465 0.00502
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995 0.00472
NM_001134407.3(GRIN2A):c.*8396T>C rs192548671 0.00319
NM_001134407.3(GRIN2A):c.1122+16T>A rs149886469 0.00187
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175 0.00105
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086 0.00067
NM_001134407.3(GRIN2A):c.942C>T (p.Pro314=) rs145172949 0.00031
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517 0.00022
NM_001134407.3(GRIN2A):c.*7289T>A rs868376839 0.00012
NM_001134407.3(GRIN2A):c.*5112C>T rs553874602 0.00009
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg) rs183029507 0.00007
NM_001134407.3(GRIN2A):c.2331G>A (p.Leu777=) rs118035164 0.00006
NM_001134407.3(GRIN2A):c.306C>T (p.Asp102=) rs200850130 0.00006
NM_000833.5(GRIN2A):c.-210+52del rs5815566
NM_001134407.3(GRIN2A):c.*119TTG[5]
NM_001134407.3(GRIN2A):c.*2764_*2774dup
NM_001134407.3(GRIN2A):c.*2769_*2774del rs35189803
NM_001134407.3(GRIN2A):c.*3341T>C rs576585646
NM_001134407.3(GRIN2A):c.*3344G>C
NM_001134407.3(GRIN2A):c.*3523C>A rs559488090
NM_001134407.3(GRIN2A):c.-18-87C>T
NM_001134407.3(GRIN2A):c.-229_-227del rs1049072717
NM_001134407.3(GRIN2A):c.1498-44CT[5] rs111268758
NM_001134407.3(GRIN2A):c.1777+136C>A rs13331377
NM_001134407.3(GRIN2A):c.2008-32CT[6] rs113949330
NM_001134407.3(GRIN2A):c.415-38331C>A rs7190716
NM_001134407.3(GRIN2A):c.415-38619A>T rs111740140
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453

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