ClinVar Miner

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

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.2202C>G (p.Val734=) rs367543138 0.00023
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124 0.00006
NM_001134407.3(GRIN2A):c.989C>T (p.Pro330Leu) rs367543120 0.00004
NM_001134407.3(GRIN2A):c.1780C>T (p.Pro594Ser) rs367543140 0.00003
NM_001134407.3(GRIN2A):c.264C>T (p.Asp88=) rs367543127 0.00003
NM_001134407.3(GRIN2A):c.3854G>A (p.Arg1285Lys) rs367543132 0.00003
NM_001134407.3(GRIN2A):c.1161C>T (p.His387=) rs367543146 0.00002
NM_001134407.3(GRIN2A):c.1340A>T (p.Asn447Ile) rs367543145 0.00001
NM_001134407.3(GRIN2A):c.1698C>T (p.Leu566=) rs367543142 0.00001
NM_001134407.3(GRIN2A):c.38C>T (p.Pro13Leu) rs367543131 0.00001
NM_001134407.3(GRIN2A):c.426T>G (p.Ser142=) rs367543125 0.00001
NM_001134407.3(GRIN2A):c.60T>C (p.Gly20=) rs367543130 0.00001
NM_001134407.3(GRIN2A):c.80C>T (p.Ala27Val) rs367543129 0.00001
NM_001134407.3(GRIN2A):c.810A>G (p.Lys270=) rs367543122 0.00001
NM_001134407.3(GRIN2A):c.1202C>T (p.Pro401Leu) rs1489261681
NM_001134407.3(GRIN2A):c.1362A>G (p.Lys454=) rs367543144
NM_001134407.3(GRIN2A):c.1557T>C (p.Ser519=) rs367543143
NM_001134407.3(GRIN2A):c.1749A>G (p.Gly583=) rs367543141
NM_001134407.3(GRIN2A):c.205G>A (p.Val69Met) rs367543128
NM_001134407.3(GRIN2A):c.2199A>G (p.Ala733=) rs367543139
NM_001134407.3(GRIN2A):c.2639A>G (p.Lys880Arg) rs367543137
NM_001134407.3(GRIN2A):c.2657A>G (p.Asn886Ser) rs367543136
NM_001134407.3(GRIN2A):c.3413A>T (p.Asn1138Ile) rs367543135
NM_001134407.3(GRIN2A):c.3647G>C (p.Ser1216Thr) rs367543134
NM_001134407.3(GRIN2A):c.3700T>G (p.Phe1234Val) rs367543133
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_001134407.3(GRIN2A):c.730C>T (p.Arg244Cys) rs367543123
NM_001134407.3(GRIN2A):c.909A>G (p.Ala303=) rs367543121

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