List of variants in gene GRIN2A reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met)	rs145956175	0.00105
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)	rs77029288	0.00068
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly)	rs145063086	0.00067
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=)	rs77705198	0.00059
NM_001134407.3(GRIN2A):c.666C>T (p.Ile222=)	rs143594020	0.00039
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=)	rs141912603	0.00039
NM_001134407.3(GRIN2A):c.1410T>G (p.Thr470=)	rs372058698	0.00028
NM_001134407.3(GRIN2A):c.2165C>T (p.Thr722Met)	rs376029542	0.00024
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=)	rs372083517	0.00022
NM_001134407.3(GRIN2A):c.736C>A (p.Leu246Ile)	rs555768104	0.00021
NM_001134407.3(GRIN2A):c.4330G>A (p.Val1444Ile)	rs150574045	0.00008
NM_001134407.3(GRIN2A):c.4353A>T (p.Arg1451Ser)	rs143693526	0.00008
NM_001134407.3(GRIN2A):c.989C>T (p.Pro330Leu)	rs367543120	0.00004
NM_001134407.3(GRIN2A):c.1069G>A (p.Val357Met)	rs78929970	0.00001
NM_001134407.3(GRIN2A):c.1265T>C (p.Ile422Thr)	rs372628324	0.00001
NM_001134407.3(GRIN2A):c.1340A>T (p.Asn447Ile)	rs367543145	0.00001
NM_001134407.3(GRIN2A):c.1812T>A (p.Ala604=)	rs760972725	0.00001
NM_001134407.3(GRIN2A):c.3722G>A (p.Arg1241Gln)	rs886042648	0.00001
NM_001134407.3(GRIN2A):c.4176A>G (p.Pro1392=)	rs886043681	0.00001
NM_001134407.3(GRIN2A):c.678C>T (p.Val226=)	rs1567187672	0.00001
NM_001134407.3(GRIN2A):c.1342G>A (p.Glu448Lys)	rs368026708
NM_001134407.3(GRIN2A):c.2415C>T (p.Asn805=)	rs777235967
NM_001134407.3(GRIN2A):c.2517C>A (p.His839Gln)	rs769482103
NM_001134407.3(GRIN2A):c.2894C>T (p.Thr965Ile)	rs886042323
NM_001134407.3(GRIN2A):c.406G>T (p.Ala136Ser)	rs1555491437
NM_001134407.3(GRIN2A):c.89G>A (p.Gly30Asp)	rs1567354651

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