ClinVar Miner

List of variants in gene GRIN2A reported by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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Gene type:
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Total variants: 40
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HGVS dbSNP
NM_000833.5(GRIN2A):c.1069G>A (p.Val357Met) rs78929970
NM_000833.5(GRIN2A):c.1453del (p.His485fs) rs1555494781
NM_000833.5(GRIN2A):c.1812T>A (p.Ala604=) rs760972725
NM_000833.5(GRIN2A):c.2415C>T (p.Asn805=) rs777235967
NM_000833.5(GRIN2A):c.2890del (p.Gln964fs) rs886042168
NM_000833.5(GRIN2A):c.2894C>T (p.Thr965Ile) rs886042323
NM_000833.5(GRIN2A):c.3722G>A (p.Arg1241Gln) rs886042648
NM_000833.5(GRIN2A):c.3813G>A (p.Trp1271Ter) rs886043129
NM_000833.5(GRIN2A):c.406G>T (p.Ala136Ser) rs1555491437
NM_000833.5(GRIN2A):c.989C>T (p.Pro330Leu) rs367543120
NM_001134407.3(GRIN2A):c.1007+1G>A rs397518465
NM_001134407.3(GRIN2A):c.1251C>T (p.Val417=) rs139329447
NM_001134407.3(GRIN2A):c.1265T>C (p.Ile422Thr)
NM_001134407.3(GRIN2A):c.1340A>T (p.Asn447Ile) rs367543145
NM_001134407.3(GRIN2A):c.1342G>A (p.Glu448Lys)
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175
NM_001134407.3(GRIN2A):c.1410T>G (p.Thr470=) rs372058698
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806
NM_001134407.3(GRIN2A):c.2146G>A (p.Ala716Thr) rs762659685
NM_001134407.3(GRIN2A):c.2165C>T (p.Thr722Met) rs376029542
NM_001134407.3(GRIN2A):c.2517C>A (p.His839Gln)
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2852G>T (p.Gly951Val) rs139795367
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_001134407.3(GRIN2A):c.4176A>G (p.Pro1392=) rs886043681
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_001134407.3(GRIN2A):c.4330G>A (p.Val1444Ile) rs150574045
NM_001134407.3(GRIN2A):c.4353A>T (p.Arg1451Ser) rs143693526
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464
NM_001134407.3(GRIN2A):c.666C>T (p.Ile222=) rs143594020
NM_001134407.3(GRIN2A):c.678C>T (p.Val226=) rs1567187672
NM_001134407.3(GRIN2A):c.736C>A (p.Leu246Ile)
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=) rs141912603
NM_001134407.3(GRIN2A):c.89G>A (p.Gly30Asp) rs1567354651
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448

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