ClinVar Miner

List of variants in gene GRIN2A reported by Fulgent Genetics, Fulgent Genetics

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Gene type:
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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465 0.00502
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464 0.00322
NM_001134407.3(GRIN2A):c.3505C>T (p.Arg1169Trp) rs369878342 0.00005
NM_001134407.3(GRIN2A):c.2650G>A (p.Asp884Asn) rs777684328 0.00002
NM_001134407.3(GRIN2A):c.3338C>T (p.Pro1113Leu) rs201698049 0.00002
NM_001134407.3(GRIN2A):c.1030G>C (p.Asp344His) rs777505684 0.00001
NM_001134407.3(GRIN2A):c.1279G>C (p.Glu427Gln) rs560839364 0.00001
NM_001134407.3(GRIN2A):c.2378C>T (p.Thr793Ile) rs893189529
NM_001134407.3(GRIN2A):c.2415C>T (p.Asn805=) rs777235967
NM_001134407.3(GRIN2A):c.2801T>C (p.Met934Thr) rs540019898
NM_001134407.3(GRIN2A):c.2933A>T (p.Tyr978Phe) rs948782419
NM_001134407.3(GRIN2A):c.3026G>A (p.Arg1009Lys) rs1900786503
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453

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