ClinVar Miner

List of variants in gene GRIN1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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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.1513C>T (p.Leu505=) rs139637382 0.00051
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.696C>T (p.Tyr232=) rs200390848 0.00006
NM_007327.4(GRIN1):c.1776C>T (p.Asn592=) rs369596145 0.00002
NM_007327.4(GRIN1):c.2223G>C (p.Ser741=) rs767848286 0.00002
NM_007327.4(GRIN1):c.1149C>T (p.Gly383=) rs138398771 0.00001
NM_007327.4(GRIN1):c.1566G>A (p.Glu522=) rs200342470 0.00001
NM_007327.4(GRIN1):c.264C>T (p.Tyr88=) rs199679287 0.00001
NM_007327.4(GRIN1):c.1380C>T (p.Ile460=)
NM_007327.4(GRIN1):c.2247T>C (p.Thr749=) rs754870278
NM_007327.4(GRIN1):c.231G>A (p.Ser77=) rs1219867246
NM_007327.4(GRIN1):c.2331C>T (p.Leu777=)
NM_007327.4(GRIN1):c.2472C>A (p.Ile824=) rs143098819
NM_007327.4(GRIN1):c.2533C>A (p.Arg845=)
NM_007327.4(GRIN1):c.750C>T (p.Gly250=)
NM_007327.4(GRIN1):c.756C>A (p.Arg252=)
NM_007327.4(GRIN1):c.849C>T (p.Asp283=)
NM_007327.4(GRIN1):c.968+10dup rs777548072

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