Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13866000A>C | CA384054478 | GRIN2B | c.209T>G (p.Leu70Arg) | |
12 | g.13866000A>G | CA384054480 | GRIN2B | c.209T>C (p.Leu70Pro) | |
12 | g.13866000A>T | CA384054482 | GRIN2B | c.209T>A (p.Leu70Gln) | |
12 | g.13866001G>A | CA478853872 | GRIN2B | c.208C>T (p.Leu70=) | |
12 | g.13866001G>C | CA384054486 | GRIN2B | c.208C>G (p.Leu70Val) | |
12 | g.13866001G>T | CA384054484 | GRIN2B | c.208C>A (p.Leu70Met) | |
12 | g.13866002T>A | CA384054489 | GRIN2B | c.207A>T (p.Glu69Asp) | |
12 | g.13866002T>C | CA478853873 | GRIN2B | c.207A>G (p.Glu69=) | |
12 | g.13866002T>G | CA384054491 | GRIN2B | c.207A>C (p.Glu69Asp) | |
12 | g.13866003T>A | CA384054494 | GRIN2B | c.206A>T (p.Glu69Val) | gnomAD v4 |
12 | g.13866003T>C | CA384054495 | GRIN2B | c.206A>G (p.Glu69Gly) | |
12 | g.13866003T>G | CA384054496 | GRIN2B | c.206A>C (p.Glu69Ala) | |
12 | g.13866004C>A | CA384054498 | GRIN2B | c.205G>T (p.Glu69Ter) | dbSNP |
12 | g.13866004C= | CA2017578225 | GRIN2B | c.205G= (p.Glu69=) | |
12 | g.13866004C>G | CA384054500 | GRIN2B | c.205G>C (p.Glu69Gln) | |
12 | g.13866004C>T | CA384054502 | GRIN2B | c.205G>A (p.Glu69Lys) | dbSNP |
12 | g.13866005C>A | CA478853874 | GRIN2B | c.204G>T (p.Val68=) | |
12 | g.13866005C>G | CA478853875 | GRIN2B | c.204G>C (p.Val68=) | |
12 | g.13866005C>T | CA478853876 | GRIN2B | c.204G>A (p.Val68=) | gnomAD v4 |
12 | g.13866006A= | CA2017578226 | GRIN2B | c.203T= (p.Val68=) | |
12 | g.13866006A>C | CA384054504 | GRIN2B | c.203T>G (p.Val68Gly) | dbSNP |
12 | g.13866006A>G | CA384054506 | GRIN2B | c.203T>C (p.Val68Ala) | |
12 | g.13866006A>T | CA384054508 | GRIN2B | c.203T>A (p.Val68Glu) | |
12 | g.13866007C>A | CA384054514 | GRIN2B | c.202G>T (p.Val68Leu) | |
12 | g.13866007C= | CA2017578227 | GRIN2B | c.202G= (p.Val68=) | |
12 | g.13866007C>G | CA384054512 | GRIN2B | c.202G>C (p.Val68Leu) | |
12 | g.13866007C>T | CA384054510 | GRIN2B | c.202G>A (p.Val68Met) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.13866008C>A | CA478853879 | GRIN2B | c.201G>T (p.Arg67=) | COSMIC |
12 | g.13866008C>G | CA478853877 | GRIN2B | c.201G>C (p.Arg67=) | |
12 | g.13866008C>T | CA478853878 | GRIN2B | c.201G>A (p.Arg67=) | |
12 | g.13866009C>A | CA384054515 | GRIN2B | c.200G>T (p.Arg67Leu) | |
12 | g.13866009C= | CA2017578228 | GRIN2B | c.200G= (p.Arg67=) | |
12 | g.13866009C>G | CA384054516 | GRIN2B | c.200G>C (p.Arg67Pro) | |
12 | g.13866009C>T | CA233148009 | GRIN2B | c.200G>A (p.Arg67Gln) | ClinVar dbSNP gnomAD v4 |
12 | g.13866010G>A | CA233148010 | GRIN2B | c.199C>T (p.Arg67Trp) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
12 | g.13866010G>C | CA384054519 | GRIN2B | c.199C>G (p.Arg67Gly) | |
12 | g.13866010G= | CA2017578229 | GRIN2B | c.199C= (p.Arg67=) | |
12 | g.13866010G>T | CA478853880 | GRIN2B | c.199C>A (p.Arg67=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
12 | g.13866011G>A | CA478853881 | GRIN2B | c.198C>T (p.Pro66=) | |
12 | g.13866011G>C | CA478853882 | GRIN2B | c.198C>G (p.Pro66=) | |
12 | g.13866011G>T | CA478853883 | GRIN2B | c.198C>A (p.Pro66=) | COSMIC |
12 | g.13866012G>A | CA384054524 | GRIN2B | c.197C>T (p.Pro66Leu) | COSMIC |
12 | g.13866012G>C | CA384054522 | GRIN2B | c.197C>G (p.Pro66Arg) | |
12 | g.13866012G>T | CA384054520 | GRIN2B | c.197C>A (p.Pro66His) | gnomAD v4 |
12 | g.13866013G>A | CA384054526 | GRIN2B | c.196C>T (p.Pro66Ser) | ClinVar dbSNP gnomAD v4 |
12 | g.13866013G>C | CA384054528 | GRIN2B | c.196C>G (p.Pro66Ala) | |
12 | g.13866013G= | CA2017578230 | GRIN2B | c.196C= (p.Pro66=) | |
12 | g.13866013G>T | CA384054530 | GRIN2B | c.196C>A (p.Pro66Thr) | |
12 | g.13866014T>A | CA478853884 | GRIN2B | c.195A>T (p.Val65=) | |
12 | g.13866014T>C | CA478853885 | GRIN2B | c.195A>G (p.Val65=) |