ClinVar Miner

List of variants in gene GRIA3 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000828.4(GRIA3):c.-2G= rs58044961 1.00000
NM_007325.5(GRIA3):c.1293+48C>T rs504096 0.59216
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.268+75T>C rs2269551 0.34082
NM_007325.5(GRIA3):c.696+170A>G rs11796015 0.14796
NM_007325.5(GRIA3):c.*2+311C>T rs148205410 0.01726
NM_007325.5(GRIA3):c.1501-204C>G rs116522013 0.01599
NM_007325.5(GRIA3):c.15G>A (p.Lys5=) rs61740996 0.01027
NM_007325.5(GRIA3):c.1080+20A>C rs73553764 0.01010
NM_007325.5(GRIA3):c.1501-8T>A rs139058646 0.00969
NM_007325.5(GRIA3):c.751-42A>G rs2297746 0.00813
NM_007325.5(GRIA3):c.109+274C>T rs112616639 0.00268
NM_007325.5(GRIA3):c.913-15A>G rs372811132 0.00131
NM_007325.5(GRIA3):c.1166A>C (p.Lys389Thr) rs146022384 0.00091
NM_007325.5(GRIA3):c.159T>C (p.Phe53=) rs145583732 0.00091
NM_007325.5(GRIA3):c.397G>A (p.Ala133Thr) rs151086692 0.00081
NM_007325.5(GRIA3):c.1181G>A (p.Arg394Gln) rs138817389 0.00063
NM_007325.5(GRIA3):c.2097C>T (p.Tyr699=) rs184185835 0.00041
NM_007325.5(GRIA3):c.696+35T>C rs367767503 0.00041
NM_007325.5(GRIA3):c.390C>T (p.Pro130=) rs142947328 0.00040
NM_007325.5(GRIA3):c.1326T>C (p.His442=) rs150823812 0.00025
NM_007325.5(GRIA3):c.*2+26T>G rs201725362 0.00021
NM_007325.5(GRIA3):c.697-29G>A rs201671470 0.00021
NM_007325.5(GRIA3):c.-17T>C rs374449092 0.00018
NM_007325.5(GRIA3):c.87A>T (p.Gly29=) rs765395672 0.00013
NM_007325.5(GRIA3):c.1185+9C>A rs763020411 0.00010
NM_007325.5(GRIA3):c.1440T>C (p.Tyr480=) rs756780145 0.00006
NM_007325.5(GRIA3):c.1772G>A (p.Arg591His) rs769866687 0.00003
NM_007325.5(GRIA3):c.342C>T (p.Thr114=) rs766567391 0.00002
NM_007325.5(GRIA3):c.1080+21T>C rs776696269 0.00001
NC_000023.11:g.123183981del rs372242931
NC_000023.11:g.123184096CT[18] rs3074025
NC_000023.11:g.123184096CT[21] rs3074025
NC_000023.11:g.123184096CT[22] rs3074025
NC_000023.11:g.123184096CT[23] rs3074025
NC_000023.11:g.123184096CT[24] rs3074025
NC_000023.11:g.123184096CT[25] rs3074025
NM_007325.5(GRIA3):c.*2+80del rs199682384
NM_007325.5(GRIA3):c.110-12C>G
NM_007325.5(GRIA3):c.110-315del rs3216834
NM_007325.5(GRIA3):c.1125T>C (p.Tyr375=) rs562407134
NM_007325.5(GRIA3):c.1294-170del rs374514027
NM_007325.5(GRIA3):c.1500+11del rs774804573
NM_007325.5(GRIA3):c.1501-13dup rs1556317771
NM_007325.5(GRIA3):c.1501-4del
NM_007325.5(GRIA3):c.1501-4dup
NM_007325.5(GRIA3):c.1581C>T (p.Ser527=)
NM_007325.5(GRIA3):c.1837T>C (p.Leu613=)
NM_007325.5(GRIA3):c.1977G>A (p.Glu659=)
NM_007325.5(GRIA3):c.2076+158C>T rs637574
NM_007325.5(GRIA3):c.2127G>A (p.Ala709=)
NM_007325.5(GRIA3):c.2323= (p.Arg775=)
NM_007325.5(GRIA3):c.268+171T>A rs73229252
NM_007325.5(GRIA3):c.269-218A>G rs3747322
NM_007325.5(GRIA3):c.508+249A>T rs4825474
NM_007325.5(GRIA3):c.509-244A>C rs5911590
NM_007325.5(GRIA3):c.577G>A (p.Val193Met)
NM_007325.5(GRIA3):c.696+172_696+173del rs56808544
NM_007325.5(GRIA3):c.696+173del rs56808544
NM_007325.5(GRIA3):c.907C>T (p.Leu303=)

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