List of variants in gene GRIA3 reported as uncertain significance by Ambry Genetics

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_007325.5(GRIA3):c.397G>A (p.Ala133Thr)	rs151086692	0.00081
NM_007325.5(GRIA3):c.430G>A (p.Ala144Thr)	rs1267207491	0.00009
NM_007325.5(GRIA3):c.419A>G (p.Gln140Arg)	rs771205448	0.00004
NM_007325.5(GRIA3):c.696+5G>A	rs748084966	0.00002
NM_007325.5(GRIA3):c.69G>C (p.Leu23Phe)	rs759740734	0.00002
NM_007325.5(GRIA3):c.967T>C (p.Tyr323His)	rs755997178	0.00002
NM_007325.5(GRIA3):c.40G>A (p.Ala14Thr)	rs1443326387	0.00001
NM_007325.5(GRIA3):c.647G>A (p.Arg216Gln)	rs753214982	0.00001
NM_007325.5(GRIA3):c.1009G>A (p.Ala337Thr)
NM_007325.5(GRIA3):c.159T>G (p.Phe53Leu)	rs145583732
NM_007325.5(GRIA3):c.1755CAA[1] (p.Asn587del)	rs2045543461
NM_007325.5(GRIA3):c.1794T>A (p.Asp598Glu)
NM_007325.5(GRIA3):c.1850T>C (p.Met617Thr)	rs1569433312
NM_007325.5(GRIA3):c.1878-3T>C
NM_007325.5(GRIA3):c.1940C>T (p.Ser647Phe)	rs1556319965
NM_007325.5(GRIA3):c.1952A>G (p.Asn651Ser)	rs2045599275
NM_007325.5(GRIA3):c.1957G>A (p.Ala653Thr)	rs1057521721
NM_007325.5(GRIA3):c.1980G>C (p.Arg660Ser)	rs988146631
NM_007325.5(GRIA3):c.20T>C (p.Met7Thr)
NM_007325.5(GRIA3):c.2132C>A (p.Pro711Gln)
NM_007325.5(GRIA3):c.2219T>C (p.Met740Thr)	rs1569441267
NM_007325.5(GRIA3):c.2321T>C (p.Leu774Ser)	rs1556334045
NM_007325.5(GRIA3):c.527C>G (p.Ala176Gly)
NM_007325.5(GRIA3):c.770T>C (p.Leu257Pro)
NM_007325.5(GRIA3):c.997C>T (p.Arg333Trp)

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