ClinVar Miner

List of variants in gene GRIA3 reported as uncertain significance for X-linked disease

Included ClinVar conditions (275):
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_007325.5(GRIA3):c.813G>C (p.Gln271His) rs756316953 0.00004
NM_007325.5(GRIA3):c.424C>T (p.Arg142Cys) rs775540855 0.00001
NM_007325.5(GRIA3):c.527C>T (p.Ala176Val) rs764670975 0.00001
NM_000828.5(GRIA3):c.2399A>G (p.Tyr800Cys)
NM_007325.5(GRIA3):c.1209A>C (p.Glu403Asp) rs2045453992
NM_007325.5(GRIA3):c.1261G>C (p.Glu421Gln)
NM_007325.5(GRIA3):c.1531A>G (p.Ile511Val)
NM_007325.5(GRIA3):c.1581C>A (p.Ser527Arg)
NM_007325.5(GRIA3):c.1679T>C (p.Val560Ala)
NM_007325.5(GRIA3):c.1701C>A (p.Ser567Arg) rs398123524
NM_007325.5(GRIA3):c.2098G>A (p.Glu700Lys) rs2045826576
NM_007325.5(GRIA3):c.2116A>C (p.Met706Leu) rs1569441235
NM_007325.5(GRIA3):c.2171G>A (p.Arg724Gln)
NM_007325.5(GRIA3):c.2189G>C (p.Gly730Ala) rs866395967
NM_007325.5(GRIA3):c.2408G>A (p.Gly803Glu) rs1569442989
NM_007325.5(GRIA3):c.2447C>T (p.Thr816Ile) rs1569443329
NM_007325.5(GRIA3):c.268+16792G>A rs1927781157
NM_007325.5(GRIA3):c.536A>G (p.Glu179Gly)
NM_007325.5(GRIA3):c.69G>A (p.Leu23=) rs759740734
NM_007325.5(GRIA3):c.783G>A (p.Met261Ile)
NM_007325.5(GRIA3):c.812A>G (p.Gln271Arg) rs2045406349
NM_007325.5(GRIA3):c.826G>C (p.Glu276Gln) rs2147378779
NM_007325.5(GRIA3):c.949A>G (p.Ile317Val) rs2147381088

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