ClinVar Miner

List of variants in gene GRIN1 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
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HGVS dbSNP gnomAD frequency
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.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.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.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.246C>T (p.Leu82=) rs192006771 0.00004
NM_007327.4(GRIN1):c.2499C>T (p.Ile833=) rs146086141 0.00004
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.1566G>A (p.Glu522=) rs200342470 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.1198-3del rs762423431
NM_007327.4(GRIN1):c.1398G>A (p.Leu466=) rs756939653
NM_007327.4(GRIN1):c.2511C>T (p.Tyr837=) rs1478532319
NM_007327.4(GRIN1):c.2520C>T (p.His840=)
NM_007327.4(GRIN1):c.474C>T (p.Tyr158=) rs1564345160
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

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