ClinVar Miner

List of variants in gene GRIN1 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
NM_007327.4(GRIN1):c.1595C>A (p.Pro532His) rs1064795158
NM_007327.4(GRIN1):c.1607A>G (p.Gln536Arg) rs1064795337
NM_007327.4(GRIN1):c.1670C>T (p.Pro557Leu) rs878853143
NM_007327.4(GRIN1):c.1910C>T (p.Ala637Val) rs1554770221
NM_007327.4(GRIN1):c.1924A>C (p.Ile642Leu) rs1064795455
NM_007327.4(GRIN1):c.1949A>T (p.Asn650Ile) rs1131691590
NM_007327.4(GRIN1):c.1974C>G (p.Asp658Glu) rs1064795712
NM_007327.4(GRIN1):c.1979C>T (p.Pro660Leu) rs1328780843
NM_007327.4(GRIN1):c.2008C>A (p.Pro670Thr) rs1057520055
NM_007327.4(GRIN1):c.2021A>T (p.Asn674Ile)
NM_007327.4(GRIN1):c.2062T>C (p.Ser688Pro) rs1131691576
NM_007327.4(GRIN1):c.2441C>A (p.Ala814Asp) rs1131691870
NM_007327.4(GRIN1):c.2530C>T (p.Arg844Cys) rs1554770667
NM_007327.4(GRIN1):c.329C>T (p.Thr110Ile) rs1064794987

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.