ClinVar Miner

List of variants in gene GRIN1 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_007327.4(GRIN1):c.1467+8G>A rs10747050 0.95319
NM_007327.4(GRIN1):c.789A>G (p.Pro263=) rs6293 0.23665
NM_007327.4(GRIN1):c.855G>A (p.Val285=) rs1126442 0.23587
NM_007327.4(GRIN1):c.2241G>C (p.Val747=) rs116354349 0.01638
NM_007327.4(GRIN1):c.2244G>C (p.Thr748=) rs79570612 0.01637
NM_007327.4(GRIN1):c.1548G>A (p.Pro516=) rs75783429 0.00518
NM_007327.4(GRIN1):c.1584G>A (p.Glu528=) rs116006955 0.00510
NM_007327.4(GRIN1):c.525G>A (p.Ala175=) rs77812749 0.00163
NM_007327.4(GRIN1):c.1809G>C (p.Leu603=) rs141249927 0.00153
NM_007327.4(GRIN1):c.768G>C (p.Gly256=) rs141473515 0.00059
NM_007327.4(GRIN1):c.1513C>T (p.Leu505=) rs139637382 0.00051
NM_007327.4(GRIN1):c.1044C>T (p.Phe348=) rs143483243 0.00026
NM_007327.4(GRIN1):c.1331C>T (p.Pro444Leu) rs200225692 0.00026
NM_007327.4(GRIN1):c.2799C>T (p.Ser933=) rs201012245 0.00026
NM_007327.4(GRIN1):c.693A>C (p.Val231=) rs201818201 0.00025
NM_007327.4(GRIN1):c.1005T>C (p.Thr335=) rs145176345 0.00023
NM_007327.4(GRIN1):c.2214C>T (p.Phe738=) rs367543116 0.00018
NM_007327.4(GRIN1):c.2097G>C (p.Leu699=) rs143865216 0.00016
NM_007327.4(GRIN1):c.1012G>A (p.Val338Met) rs140672142 0.00015
NM_007327.4(GRIN1):c.1340C>A (p.Pro447His) rs587780348 0.00014
NM_007327.4(GRIN1):c.2235C>T (p.Asp745=) rs200518957 0.00010
NM_007327.4(GRIN1):c.1995G>C (p.Thr665=) rs200127557 0.00009
NM_007327.4(GRIN1):c.2298C>T (p.Ser766=) rs138298331 0.00009
NM_007327.4(GRIN1):c.610G>A (p.Val204Met) rs140422926 0.00009
NM_007327.4(GRIN1):c.1255A>G (p.Thr419Ala) rs763133592 0.00008
NM_007327.4(GRIN1):c.1263G>A (p.Lys421=) rs199588413 0.00006
NM_007327.4(GRIN1):c.546G>A (p.Thr182=) rs77854056 0.00006
NM_007327.4(GRIN1):c.696C>T (p.Tyr232=) rs200390848 0.00006
NM_007327.4(GRIN1):c.705C>T (p.Ala235=) rs201343933 0.00006
NM_007327.4(GRIN1):c.467G>A (p.Arg156His) rs762490192 0.00005
NM_007327.4(GRIN1):c.1113C>T (p.His371=) rs150508714 0.00004
NM_007327.4(GRIN1):c.246C>T (p.Leu82=) rs192006771 0.00004
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=) rs146086141 0.00004
NM_007327.4(GRIN1):c.1045G>T (p.Ala349Ser) rs148008303 0.00003
NM_007327.4(GRIN1):c.1382A>G (p.Asp461Gly) rs955781126 0.00003
NM_007327.4(GRIN1):c.614C>T (p.Thr205Met) rs201592328 0.00003
NM_007327.4(GRIN1):c.669C>G (p.Ala223=) rs766714775 0.00003
NM_007327.4(GRIN1):c.1449G>A (p.Lys483=) rs778957098 0.00002
NM_007327.4(GRIN1):c.1684C>T (p.Leu562=) rs1212742276 0.00002
NM_007327.4(GRIN1):c.2223G>C (p.Ser741=) rs767848286 0.00002
NM_007327.4(GRIN1):c.630G>A (p.Glu210=) rs1057522916 0.00002
NM_007327.4(GRIN1):c.1198-3C>T rs200368768 0.00001
NM_007327.4(GRIN1):c.152A>G (p.Lys51Arg) rs767000671 0.00001
NM_007327.4(GRIN1):c.1566G>A (p.Glu522=) rs200342470 0.00001
NM_007327.4(GRIN1):c.344G>A (p.Arg115His) rs774822539 0.00001
NM_007327.4(GRIN1):c.615G>A (p.Thr205=) rs770695987 0.00001
NM_007327.4(GRIN1):c.879C>T (p.His293=) rs746040843 0.00001
NM_007327.4(GRIN1):c.992C>T (p.Ala331Val) rs201324316 0.00001
NM_007327.4(GRIN1):c.1198-3C>A rs200368768
NM_007327.4(GRIN1):c.1198-3del rs762423431
NM_007327.4(GRIN1):c.1198-6C>T rs1057521991
NM_007327.4(GRIN1):c.1355C>T (p.Pro452Leu) rs1564361971
NM_007327.4(GRIN1):c.1398G>A (p.Leu466=) rs756939653
NM_007327.4(GRIN1):c.14G>A (p.Arg5His)
NM_007327.4(GRIN1):c.1550T>C (p.Leu517Pro) rs771464830
NM_007327.4(GRIN1):c.1643G>A (p.Arg548Gln) rs1554770044
NM_007327.4(GRIN1):c.1645A>C (p.Ser549Arg) rs1554770046
NM_007327.4(GRIN1):c.1778G>T (p.Ser593Ile)
NM_007327.4(GRIN1):c.1829C>G (p.Ser610Cys) rs1564363645
NM_007327.4(GRIN1):c.1852G>C (p.Gly618Arg) rs1833614590
NM_007327.4(GRIN1):c.1858G>C (p.Gly620Arg) rs797045047
NM_007327.4(GRIN1):c.1958C>G (p.Ala653Gly) rs1554770258
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) rs1328780843
NM_007327.4(GRIN1):c.2414del (p.Pro805fs) rs766786160
NM_007327.4(GRIN1):c.2420C>T (p.Thr807Ile) rs1554770590
NM_007327.4(GRIN1):c.2443G>A (p.Gly815Arg) rs797044925
NM_007327.4(GRIN1):c.2446G>A (p.Val816Ile)
NM_007327.4(GRIN1):c.2511C>T (p.Tyr837=) rs1478532319
NM_007327.4(GRIN1):c.2520C>T (p.His840=)
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys) rs1554770667
NM_007327.4(GRIN1):c.2805T>A (p.His935Gln) rs1262184514
NM_007327.4(GRIN1):c.474C>T (p.Tyr158=) rs1564345160
NM_007327.4(GRIN1):c.616G>T (p.Ala206Ser)
NM_007327.4(GRIN1):c.780C>A (p.Arg260=)
NM_007327.4(GRIN1):c.87T>C (p.Ile29=)
NM_007327.4(GRIN1):c.888C>T (p.Leu296=) rs770334644
NM_007327.4(GRIN1):c.952G>C (p.Gly318Arg)

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