Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13753506_13753526del | CA2695216106 | GRIN2B | c.804_824del (p.Val269_Thr275del) | |
12 | g.13753526_13753527del | CA16609334 | GRIN2B | c.803_804del (p.Thr268SerfsTer15) | ClinVar dbSNP |
12 | g.13753526G>A | CA478853593 | GRIN2B | c.801C>T (p.Asp267=) | |
12 | g.13753526G>C | CA384053422 | GRIN2B | c.801C>G (p.Asp267Glu) | |
12 | g.13753526G>T | CA384053424 | GRIN2B | c.801C>A (p.Asp267Glu) | |
12 | g.13753527T>A | CA384053426 | GRIN2B | c.800A>T (p.Asp267Val) | |
12 | g.13753527T>C | CA384053427 | GRIN2B | c.800A>G (p.Asp267Gly) | |
12 | g.13753527T>G | CA384053430 | GRIN2B | c.800A>C (p.Asp267Ala) | |
12 | g.13753528C>A | CA384053431 | GRIN2B | c.799G>T (p.Asp267Tyr) | |
12 | g.13753528C>G | CA384053433 | GRIN2B | c.799G>C (p.Asp267His) | |
12 | g.13753528C>T | CA384053434 | GRIN2B | c.799G>A (p.Asp267Asn) | |
12 | g.13753529T>A | CA478853594 | GRIN2B | c.798A>T (p.Thr266=) | |
12 | g.13753529T>C | CA478853595 | GRIN2B | c.798A>G (p.Thr266=) | |
12 | g.13753529T>G | CA478853596 | GRIN2B | c.798A>C (p.Thr266=) | |
12 | g.13753530G>A | CA6461364 | GRIN2B | c.797C>T (p.Thr266Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753530G>C | CA384053438 | GRIN2B | c.797C>G (p.Thr266Arg) | |
12 | g.13753530G= | CA2017525870 | GRIN2B | c.797C= (p.Thr266=) | |
12 | g.13753530G>T | CA384053435 | GRIN2B | c.797C>A (p.Thr266Lys) | |
12 | g.13753531T>A | CA384053440 | GRIN2B | c.796A>T (p.Thr266Ser) | |
12 | g.13753531T>C | CA233115845 | GRIN2B | c.796A>G (p.Thr266Ala) | dbSNP |
12 | g.13753531T>G | CA384053441 | GRIN2B | c.796A>C (p.Thr266Pro) | |
12 | g.13753531T= | CA2017525871 | GRIN2B | c.796A= (p.Thr266=) | |
12 | g.13753532A>C | CA384053442 | GRIN2B | c.795T>G (p.Asp265Glu) | |
12 | g.13753532A>G | CA478853598 | GRIN2B | c.795T>C (p.Asp265=) | |
12 | g.13753532A>T | CA384053444 | GRIN2B | c.795T>A (p.Asp265Glu) | |
12 | g.13753533T>A | CA384053446 | GRIN2B | c.794A>T (p.Asp265Val) | |
12 | g.13753533T>C | CA384053448 | GRIN2B | c.794A>G (p.Asp265Gly) | |
12 | g.13753533T>G | CA384053452 | GRIN2B | c.794A>C (p.Asp265Ala) | |
12 | g.13753534C>A | CA384053454 | GRIN2B | c.793G>T (p.Asp265Tyr) | |
12 | g.13753534C>G | CA384053455 | GRIN2B | c.793G>C (p.Asp265His) | |
12 | g.13753534C>T | CA384053456 | GRIN2B | c.793G>A (p.Asp265Asn) | COSMIC |
12 | g.13753535C>A | CA478853600 | GRIN2B | c.792G>T (p.Gly264=) | COSMIC |
12 | g.13753535C= | CA2017525872 | GRIN2B | c.792G= (p.Gly264=) | |
12 | g.13753535C>G | CA478853602 | GRIN2B | c.792G>C (p.Gly264=) | |
12 | g.13753535C>T | CA478853601 | GRIN2B | c.792G>A (p.Gly264=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753536C>A | CA384053459 | GRIN2B | c.791G>T (p.Gly264Val) | |
12 | g.13753536C>G | CA384053458 | GRIN2B | c.791G>C (p.Gly264Ala) | |
12 | g.13753536C>T | CA384053457 | GRIN2B | c.791G>A (p.Gly264Glu) | COSMIC |
12 | g.13753537C>A | CA384053463 | GRIN2B | c.790G>T (p.Gly264Trp) | |
12 | g.13753537C>G | CA384053460 | GRIN2B | c.790G>C (p.Gly264Arg) | |
12 | g.13753537C>T | CA384053462 | GRIN2B | c.790G>A (p.Gly264Arg) | |
12 | g.13753538T>A | CA478853603 | GRIN2B | c.789A>T (p.Ala263=) | |
12 | g.13753538T>C | CA478853604 | GRIN2B | c.789A>G (p.Ala263=) | |
12 | g.13753538T>G | CA6461365 | GRIN2B | c.789A>C (p.Ala263=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753538T= | CA2017525873 | GRIN2B | c.789A= (p.Ala263=) | |
12 | g.13753539G>A | CA384053466 | GRIN2B | c.788C>T (p.Ala263Val) | |
12 | g.13753539G>C | CA384053468 | GRIN2B | c.788C>G (p.Ala263Gly) | |
12 | g.13753539G>T | CA384053471 | GRIN2B | c.788C>A (p.Ala263Glu) | |
12 | g.13753540C>A | CA384053473 | GRIN2B | c.787G>T (p.Ala263Ser) | dbSNP |
12 | g.13753540C= | CA2017525874 | GRIN2B | c.787G= (p.Ala263=) |