ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001134407.3(GRIN2A):c.*2586C>T
NM_001134407.3(GRIN2A):c.*7650_*7654del rs537062402
NM_001134407.3(GRIN2A):c.*8536_*8537insC rs59371229
NM_001134407.3(GRIN2A):c.1007+13T>G rs199862009
NM_001134407.3(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441
NM_001134407.3(GRIN2A):c.3138A>G (p.Leu1046=) rs773244936
NM_001134407.3(GRIN2A):c.3884T>C (p.Ile1295Thr) rs757351084
NM_001134407.3(GRIN2A):c.419C>T (p.Pro140Leu) rs142566406
NM_001134407.3(GRIN2A):c.83A>C (p.Glu28Ala) rs146839931
NM_001134407.3(GRIN2A):c.963C>T (p.Tyr321=) rs368200727

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