ClinVar Miner

List of variants in gene GRIN2A reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.3535T>G (p.Ser1179Ala) rs142670870 0.00010
NM_001134407.3(GRIN2A):c.3120G>C (p.Glu1040Asp) rs756663920 0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353 0.00004
NM_001134407.3(GRIN2A):c.1271C>A (p.Pro424His) rs375260513 0.00003
NM_001134407.3(GRIN2A):c.3854G>A (p.Arg1285Lys) rs367543132 0.00003
NM_001134407.3(GRIN2A):c.1757G>A (p.Arg586Lys) rs768958947 0.00002
NM_001134407.3(GRIN2A):c.3532C>A (p.Leu1178Ile) rs377152953 0.00002
NM_001134407.3(GRIN2A):c.2566C>G (p.Arg856Gly) rs201072838 0.00001
NM_001134407.3(GRIN2A):c.3032G>A (p.Arg1011Gln) rs1163766811 0.00001
NM_001134407.3(GRIN2A):c.3052G>A (p.Val1018Met) rs775756583 0.00001
NM_001134407.3(GRIN2A):c.3619T>C (p.Tyr1207His) rs587780355 0.00001
NM_001134407.3(GRIN2A):c.1063_1065delinsCAG (p.Tyr355Gln)
NM_001134407.3(GRIN2A):c.1493G>A (p.Gly498Asp) rs749732928
NM_001134407.3(GRIN2A):c.1678ATG[1] (p.Met561del) rs1057519248
NM_001134407.3(GRIN2A):c.1778-3C>A rs1060499722
NM_001134407.3(GRIN2A):c.1783C>T (p.His595Tyr)
NM_001134407.3(GRIN2A):c.1830C>T (p.Gly610=) rs1555492787
NM_001134407.3(GRIN2A):c.1990G>A (p.Gly664Ser)
NM_001134407.3(GRIN2A):c.2069C>T (p.Thr690Met) rs1445802934
NM_001134407.3(GRIN2A):c.2091C>T (p.Asn697=) rs1400933589
NM_001134407.3(GRIN2A):c.2184C>G (p.Phe728Leu) rs773358718
NM_001134407.3(GRIN2A):c.2537G>A (p.Arg846His)
NM_001134407.3(GRIN2A):c.2627T>G (p.Ile876Ser) rs199784503
NM_001134407.3(GRIN2A):c.2644T>A (p.Ser882Thr) rs1384190116
NM_001134407.3(GRIN2A):c.2695C>A (p.Arg899=) rs796052553
NM_001134407.3(GRIN2A):c.2698T>C (p.Ser900Pro) rs1596377696
NM_001134407.3(GRIN2A):c.2830T>C (p.Ser944Pro) rs1900803126
NM_001134407.3(GRIN2A):c.2917G>A (p.Asp973Asn) rs1900795341
NM_001134407.3(GRIN2A):c.299T>C (p.Phe100Ser)
NM_001134407.3(GRIN2A):c.3073T>A (p.Ser1025Thr) rs1596376846
NM_001134407.3(GRIN2A):c.3141G>C (p.Lys1047Asn) rs770039926
NM_001134407.3(GRIN2A):c.3152A>G (p.Tyr1051Cys) rs1567277844
NM_001134407.3(GRIN2A):c.3271G>A (p.Ala1091Thr) rs2141133924
NM_001134407.3(GRIN2A):c.3335C>A (p.Ser1112Tyr) rs1436083069
NM_001134407.3(GRIN2A):c.3544G>A (p.Asp1182Asn) rs375160358
NM_001134407.3(GRIN2A):c.3652C>T (p.Leu1218Phe) rs1596375400
NM_001134407.3(GRIN2A):c.3670T>A (p.Tyr1224Asn)
NM_001134407.3(GRIN2A):c.3902A>G (p.Glu1301Gly)
NM_001134407.3(GRIN2A):c.3989G>C (p.Ser1330Thr) rs1596374624
NM_001134407.3(GRIN2A):c.398T>C (p.Met133Thr) rs1596586834
NM_001134407.3(GRIN2A):c.4052G>A (p.Ser1351Asn) rs2141127120
NM_001134407.3(GRIN2A):c.40G>A (p.Ala14Thr) rs1596587522
NM_001134407.3(GRIN2A):c.4157C>T (p.Pro1386Leu) rs1277391984
NM_001134407.3(GRIN2A):c.4205G>C (p.Arg1402Pro) rs74935155
NM_001134407.3(GRIN2A):c.4250G>A (p.Arg1417Gln) rs1346618506
NM_001134407.3(GRIN2A):c.4389T>G (p.Asp1463Glu) rs748047572
NM_001134407.3(GRIN2A):c.508T>C (p.Phe170Leu) rs1596344877
NM_001134407.3(GRIN2A):c.691T>G (p.Cys231Gly)
NM_001134407.3(GRIN2A):c.758T>C (p.Phe253Ser) rs762869573
NM_001134407.3(GRIN2A):c.769G>A (p.Val257Ile) rs2044761053
NM_001134407.3(GRIN2A):c.932C>A (p.Ser311Tyr)

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