ClinVar Miner

List of variants in gene GRIA3 studied for developmental disorder of mental health

Included ClinVar conditions (728):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000828.4(GRIA3):c.-2G= rs58044961 1.00000
NM_007325.5(GRIA3):c.751-16T>C rs550640 0.58620
NM_007325.5(GRIA3):c.1200T>C (p.Asn400=) rs502434 0.57798
NM_007325.5(GRIA3):c.1181G>A (p.Arg394Gln) rs138817389 0.00063
NM_007325.5(GRIA3):c.580G>A (p.Gly194Arg) rs189437004 0.00009
NM_007325.5(GRIA3):c.466T>C (p.Tyr156His) rs144902457 0.00005
NM_007325.5(GRIA3):c.813G>C (p.Gln271His) rs756316953 0.00004
NM_007325.5(GRIA3):c.609G>T (p.Arg203Ser) rs147567539 0.00002
NM_007325.5(GRIA3):c.1348C>T (p.Arg450Ter) rs183018401 0.00001
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.2359G>A (p.Glu787Lys)
NM_000828.5(GRIA3):c.2399A>G (p.Tyr800Cys)
NM_007325.5(GRIA3):c.1125T>C (p.Tyr375=) rs562407134
NM_007325.5(GRIA3):c.1180C>T (p.Arg394Ter) rs2147383715
NM_007325.5(GRIA3):c.1209A>C (p.Glu403Asp) rs2045453992
NM_007325.5(GRIA3):c.1261G>C (p.Glu421Gln)
NM_007325.5(GRIA3):c.1450_1453dup (p.Pro485fs) rs2147384890
NM_007325.5(GRIA3):c.1474G>A (p.Gly492Ser) rs2045463858
NM_007325.5(GRIA3):c.1531A>G (p.Ile511Val)
NM_007325.5(GRIA3):c.1544G>A (p.Arg515His)
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.1844C>T (p.Ala615Val) rs140908982
NM_007325.5(GRIA3):c.1888G>A (p.Gly630Arg) rs587777361
NM_007325.5(GRIA3):c.1888G>C (p.Gly630Arg) rs587777361
NM_007325.5(GRIA3):c.1891C>A (p.Arg631Ser) rs137852351
NM_007325.5(GRIA3):c.1949C>T (p.Ala650Val)
NM_007325.5(GRIA3):c.1957G>A (p.Ala653Thr) rs1057521721
NM_007325.5(GRIA3):c.1957G>T (p.Ala653Ser)
NM_007325.5(GRIA3):c.1964T>C (p.Phe655Ser) rs1135401788
NM_007325.5(GRIA3):c.1973T>C (p.Val658Ala)
NM_007325.5(GRIA3):c.2038_2040delinsTGT (p.Gly680Cys) rs2147401116
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.2117T>C (p.Met706Thr) rs137852352
NM_007325.5(GRIA3):c.2171G>A (p.Arg724Gln)
NM_007325.5(GRIA3):c.2189G>C (p.Gly730Ala) rs866395967
NM_007325.5(GRIA3):c.2327C>T (p.Thr776Met) rs780680047
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.2497G>A (p.Gly833Arg) rs137852350
NM_007325.5(GRIA3):c.2575C>T (p.Leu859Phe) rs2045919094
NM_007325.5(GRIA3):c.268+16757dup rs778944548
NM_007325.5(GRIA3):c.268+16762dup rs11452643
NM_007325.5(GRIA3):c.268+16792G>A rs1927781157
NM_007325.5(GRIA3):c.284C>T (p.Ser95Leu)
NM_007325.5(GRIA3):c.307G>T (p.Gly103Ter)
NM_007325.5(GRIA3):c.384dup (p.Phe129fs) rs2147282654
NM_007325.5(GRIA3):c.536A>G (p.Glu179Gly)
NM_007325.5(GRIA3):c.646C>T (p.Arg216Ter) rs139990565
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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.