ClinVar Miner

List of variants in gene GRIN2A reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 0.00007
NM_001134407.3(GRIN2A):c.559G>A (p.Val187Ile) rs751692867 0.00006
NM_001134407.3(GRIN2A):c.3363T>G (p.Asp1121Glu) rs764292783 0.00004
NM_001134407.3(GRIN2A):c.3919C>T (p.Pro1307Ser) rs148827608 0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353 0.00004
NM_001134407.3(GRIN2A):c.883G>A (p.Gly295Ser) rs568484876 0.00004
NM_001134407.3(GRIN2A):c.2024A>C (p.Asp675Ala) rs75130648 0.00003
NM_001134407.3(GRIN2A):c.2907C>G (p.Asn969Lys) rs772589363 0.00002
NM_001134407.3(GRIN2A):c.1738A>G (p.Ser580Gly) rs777029084 0.00001
NM_001134407.3(GRIN2A):c.2681T>A (p.Met894Lys) rs775144380 0.00001
NM_001134407.3(GRIN2A):c.2696G>A (p.Arg899Gln) rs759145938 0.00001
NM_001134407.3(GRIN2A):c.2752C>T (p.Pro918Ser) rs778940856 0.00001
NM_001134407.3(GRIN2A):c.2927A>G (p.Asn976Ser) rs886039239 0.00001
NM_001134407.3(GRIN2A):c.3032G>A (p.Arg1011Gln) rs1163766811 0.00001
NM_001134407.3(GRIN2A):c.3163G>C (p.Glu1055Gln) rs370107080 0.00001
NM_001134407.3(GRIN2A):c.31G>C (p.Val11Leu) rs769657047 0.00001
NM_001134407.3(GRIN2A):c.3311C>T (p.Thr1104Ile) rs755577016 0.00001
NM_001134407.3(GRIN2A):c.3522T>A (p.Asn1174Lys) rs772104446 0.00001
NM_001134407.3(GRIN2A):c.3619T>C (p.Tyr1207His) rs587780355 0.00001
NM_001134407.3(GRIN2A):c.4109C>G (p.Ser1370Cys) rs762981158 0.00001
NM_001134407.3(GRIN2A):c.4245C>A (p.Asp1415Glu) rs777328885 0.00001
NM_001134407.3(GRIN2A):c.467C>T (p.Thr156Met) rs763500409 0.00001
NM_001134407.3(GRIN2A):c.583T>C (p.Phe195Leu) rs1445598953 0.00001
NM_001134407.3(GRIN2A):c.904G>A (p.Ala302Thr) rs901717931 0.00001
NM_001134407.3(GRIN2A):c.1008-6T>G
NM_001134407.3(GRIN2A):c.100C>G (p.Leu34Val)
NM_001134407.3(GRIN2A):c.1249G>T (p.Val417Phe) rs749504561
NM_001134407.3(GRIN2A):c.1271C>T (p.Pro424Leu) rs375260513
NM_001134407.3(GRIN2A):c.1288G>A (p.Val430Met)
NM_001134407.3(GRIN2A):c.1382T>C (p.Ile461Thr) rs1567337914
NM_001134407.3(GRIN2A):c.1462A>G (p.Lys488Glu)
NM_001134407.3(GRIN2A):c.1487T>C (p.Met496Thr)
NM_001134407.3(GRIN2A):c.1651G>A (p.Glu551Lys) rs1555494671
NM_001134407.3(GRIN2A):c.1739G>T (p.Ser580Ile) rs1567332765
NM_001134407.3(GRIN2A):c.1777+6G>C rs76549675
NM_001134407.3(GRIN2A):c.2069C>T (p.Thr690Met) rs1445802934
NM_001134407.3(GRIN2A):c.2467A>G (p.Met823Val)
NM_001134407.3(GRIN2A):c.2473G>A (p.Ala825Thr)
NM_001134407.3(GRIN2A):c.2494C>T (p.Leu832Phe) rs145495027
NM_001134407.3(GRIN2A):c.2567G>A (p.Arg856Gln)
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2635AAG[2] (p.Lys881del) rs766019656
NM_001134407.3(GRIN2A):c.2663C>G (p.Thr888Arg) rs149698593
NM_001134407.3(GRIN2A):c.2771T>C (p.Phe924Ser) rs1177789326
NM_001134407.3(GRIN2A):c.2801T>C (p.Met934Thr) rs540019898
NM_001134407.3(GRIN2A):c.2842T>A (p.Ser948Thr)
NM_001134407.3(GRIN2A):c.3010T>C (p.Ser1004Pro)
NM_001134407.3(GRIN2A):c.3040T>C (p.Trp1014Arg)
NM_001134407.3(GRIN2A):c.3088C>G (p.Pro1030Ala)
NM_001134407.3(GRIN2A):c.3126G>C (p.Arg1042Ser)
NM_001134407.3(GRIN2A):c.3206C>T (p.Thr1069Met) rs777249842
NM_001134407.3(GRIN2A):c.3211C>T (p.His1071Tyr) rs1555482611
NM_001134407.3(GRIN2A):c.3215G>A (p.Arg1072Lys)
NM_001134407.3(GRIN2A):c.323C>T (p.Ala108Val)
NM_001134407.3(GRIN2A):c.3362A>G (p.Asp1121Gly)
NM_001134407.3(GRIN2A):c.3365G>C (p.Gly1122Ala)
NM_001134407.3(GRIN2A):c.3432C>A (p.Asn1144Lys)
NM_001134407.3(GRIN2A):c.3504C>G (p.Asn1168Lys)
NM_001134407.3(GRIN2A):c.3568C>T (p.His1190Tyr)
NM_001134407.3(GRIN2A):c.3590G>A (p.Gly1197Asp)
NM_001134407.3(GRIN2A):c.3637C>T (p.His1213Tyr)
NM_001134407.3(GRIN2A):c.3647G>C (p.Ser1216Thr) rs367543134
NM_001134407.3(GRIN2A):c.3909C>G (p.Asp1303Glu) rs765744766
NM_001134407.3(GRIN2A):c.4053C>A (p.Ser1351Arg)
NM_001134407.3(GRIN2A):c.4205G>C (p.Arg1402Pro) rs74935155
NM_001134407.3(GRIN2A):c.4220C>T (p.Ser1407Leu)
NM_001134407.3(GRIN2A):c.4250G>A (p.Arg1417Gln) rs1346618506
NM_001134407.3(GRIN2A):c.4354C>A (p.Arg1452Ser) rs568622613
NM_001134407.3(GRIN2A):c.4389T>G (p.Asp1463Glu) rs748047572
NM_001134407.3(GRIN2A):c.568A>G (p.Thr190Ala) rs886051634
NM_001134407.3(GRIN2A):c.670T>C (p.Ser224Pro)
NM_001134407.3(GRIN2A):c.746C>G (p.Thr249Ser)
NM_001134407.3(GRIN2A):c.851G>T (p.Trp284Leu)
NM_001134407.3(GRIN2A):c.890G>A (p.Gly297Asp) rs775591257
NM_001134407.3(GRIN2A):c.899C>T (p.Thr300Ile)
NM_001134407.3(GRIN2A):c.91C>A (p.Pro31Thr)
NM_001134407.3(GRIN2A):c.932C>A (p.Ser311Tyr)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.