ClinVar Miner

List of variants in gene GRIA3 studied for Mental retardation, X-linked, syndromic, wu type

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
GRIA3, 0.4-MB DEL
NM_007325.5(GRIA3):c.1181G>A (p.Arg394Gln) rs138817389
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.1957G>A (p.Ala653Thr) rs1057521721
NM_007325.5(GRIA3):c.1964T>C (p.Phe655Ser) rs1135401788
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.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.2497G>A (p.Gly833Arg) rs137852350
NM_007325.5(GRIA3):c.268+16757dup rs778944548
NM_007325.5(GRIA3):c.268+16762dup rs11452643
NM_007325.5(GRIA3):c.466T>C (p.Tyr156His) rs144902457
NM_007325.5(GRIA3):c.527C>T (p.Ala176Val) rs764670975
NM_007325.5(GRIA3):c.580G>A (p.Gly194Arg) rs189437004
NM_007325.5(GRIA3):c.813G>C (p.Gln271His) rs756316953

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.