ClinVar Miner

Variants in gene GRIN2A with conflicting interpretations

Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission Variants with at least 2 submissions and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any kind of conflict
468 53 0 37 28 0 6 65

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 3 3 1 0
likely pathogenic 3 0 3 0 0
uncertain significance 3 3 0 27 6
likely benign 1 0 27 0 34
benign 0 0 6 34 0

All variants with conflicting interpretations #

Total variants: 65
Download table as spreadsheet
HGVS dbSNP
NM_000833.4(GRIN2A):c.-209-11C>T rs139646156
NM_000833.4(GRIN2A):c.-34C>A rs564039694
NM_000833.4(GRIN2A):c.-34C>G rs564039694
NM_000833.4(GRIN2A):c.1069G>A (p.Val357Met) rs78929970
NM_000833.4(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009
NM_000833.4(GRIN2A):c.1251C>T (p.Val417=) rs139329447
NM_000833.4(GRIN2A):c.1275G>A (p.Leu425=) rs2229193
NM_000833.4(GRIN2A):c.1329-8C>T rs7193290
NM_000833.4(GRIN2A):c.1329-9T>G rs541442732
NM_000833.4(GRIN2A):c.1354G>A (p.Val452Met) rs145956175
NM_000833.4(GRIN2A):c.1380C>T (p.Cys460=) rs375291296
NM_000833.4(GRIN2A):c.1410T>G (p.Thr470=) rs372058698
NM_000833.4(GRIN2A):c.1553G>A (p.Arg518His) rs397518470
NM_000833.4(GRIN2A):c.1629C>T (p.Thr543=) rs758378272
NM_000833.4(GRIN2A):c.1652-13T>C rs201444481
NM_000833.4(GRIN2A):c.1777+6G>T rs76549675
NM_000833.4(GRIN2A):c.2007+10C>T rs368110989
NM_000833.4(GRIN2A):c.2069C>T (p.Thr690Met) rs1445802934
NM_000833.4(GRIN2A):c.2085G>C (p.Arg695=) rs9806806
NM_000833.4(GRIN2A):c.2146G>A (p.Ala716Thr) rs762659685
NM_000833.4(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382
NM_000833.4(GRIN2A):c.2197G>A (p.Ala733Thr) rs796052550
NM_000833.4(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_000833.4(GRIN2A):c.2277C>T (p.Thr759=) rs148846694
NM_000833.4(GRIN2A):c.2325C>T (p.Ile775=) rs748291723
NM_000833.4(GRIN2A):c.2346_2356+8delTGTGGGTGATGGTAAGACC rs1064795143
NM_000833.4(GRIN2A):c.2441T>C (p.Ile814Thr) rs780654733
NM_000833.4(GRIN2A):c.2452G>A (p.Ala818Thr) rs1555483699
NM_000833.4(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_000833.4(GRIN2A):c.2664G>A (p.Thr888=) rs113847665
NM_000833.4(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
NM_000833.4(GRIN2A):c.2735C>G (p.Ser912Cys) rs200588845
NM_000833.4(GRIN2A):c.2760A>G (p.Arg920=) rs80138441
NM_000833.4(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_000833.4(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465
NM_000833.4(GRIN2A):c.2927A>G (p.Asn976Ser) rs886039239
NM_000833.4(GRIN2A):c.3064C>T (p.Arg1022Cys) rs560057284
NM_000833.4(GRIN2A):c.306C>T (p.Asp102=) rs200850130
NM_000833.4(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_000833.4(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995
NM_000833.4(GRIN2A):c.3363T>G (p.Asp1121Glu) rs764292783
NM_000833.4(GRIN2A):c.3400C>A (p.Gln1134Lys) rs748967552
NM_000833.4(GRIN2A):c.3622C>A (p.Arg1208=) rs78544202
NM_000833.4(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517
NM_000833.4(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_000833.4(GRIN2A):c.3884T>C (p.Ile1295Thr) rs757351084
NM_000833.4(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067
NM_000833.4(GRIN2A):c.4176A>G (p.Pro1392=) rs886043681
NM_000833.4(GRIN2A):c.4185G>A (p.Ala1395=) rs778429009
NM_000833.4(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_000833.4(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_000833.4(GRIN2A):c.447G>A (p.Ala149=) rs144464666
NM_000833.4(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353
NM_000833.4(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464
NM_000833.4(GRIN2A):c.666C>T (p.Ile222=) rs143594020
NM_000833.4(GRIN2A):c.669C>T (p.His223=) rs138117658
NM_000833.4(GRIN2A):c.702C>T (p.Asp234=) rs150208429
NM_000833.4(GRIN2A):c.741C>T (p.Gly247=) rs141912603
NM_000833.4(GRIN2A):c.747C>T (p.Thr249=) rs774169125
NM_000833.4(GRIN2A):c.76G>T (p.Ala26Ser) rs751198815
NM_000833.4(GRIN2A):c.819A>G (p.Pro273=) rs148085725
NM_000833.4(GRIN2A):c.882C>T (p.Asp294=) rs201002710
NM_000833.4(GRIN2A):c.900C>T (p.Thr300=) rs143669998
NM_000833.4(GRIN2A):c.903C>T (p.Thr301=) rs78241448
NM_000833.4(GRIN2A):c.939C>T (p.Ile313=) rs146867324

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