ClinVar Miner

List of variants in gene GRIA3 reported as uncertain significance for Inborn genetic diseases

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_007325.5(GRIA3):c.1878-3T>C rs373419006 0.00007
NM_007325.5(GRIA3):c.430G>A (p.Ala144Thr) rs1267207491 0.00007
NM_007325.5(GRIA3):c.419A>G (p.Gln140Arg) rs771205448 0.00004
NM_007325.5(GRIA3):c.106A>G (p.Ile36Val) rs764200669 0.00002
NM_007325.5(GRIA3):c.2219T>C (p.Met740Thr) rs1569441267 0.00002
NM_007325.5(GRIA3):c.647G>A (p.Arg216Gln) rs753214982 0.00002
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.742G>A (p.Ala248Thr) rs1183014762 0.00002
NM_007325.5(GRIA3):c.967T>C (p.Tyr323His) rs755997178 0.00002
NM_007325.5(GRIA3):c.1259C>T (p.Ser420Leu) rs2045454264 0.00001
NM_007325.5(GRIA3):c.40G>A (p.Ala14Thr) rs1443326387 0.00001
NM_007325.5(GRIA3):c.770T>C (p.Leu257Pro) rs138419523 0.00001
NM_007325.5(GRIA3):c.1009G>A (p.Ala337Thr) rs2521156437
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) rs2521209666
NM_007325.5(GRIA3):c.1795C>G (p.Pro599Ala)
NM_007325.5(GRIA3):c.1850T>C (p.Met617Thr) rs1569433312
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.1980G>C (p.Arg660Ser) rs988146631
NM_007325.5(GRIA3):c.20T>C (p.Met7Thr) rs2520418046
NM_007325.5(GRIA3):c.2132C>A (p.Pro711Gln) rs1251959475
NM_007325.5(GRIA3):c.2321T>C (p.Leu774Ser) rs1556334045
NM_007325.5(GRIA3):c.2642G>C (p.Arg881Thr) rs2521368617
NM_007325.5(GRIA3):c.2656G>A (p.Val886Met)
NM_007325.5(GRIA3):c.38G>A (p.Arg13Gln) rs2520418302
NM_007325.5(GRIA3):c.527C>G (p.Ala176Gly) rs764670975
NM_007325.5(GRIA3):c.992T>C (p.Val331Ala) rs921385861
NM_007325.5(GRIA3):c.997C>T (p.Arg333Trp) rs2521156381

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