| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.13753879T>A | CA384054819 | GRIN2B | c.448A>T (p.Ile150Phe) | |
| 12 | g.13753879T>C | CA315046 | GRIN2B | c.448A>G (p.Ile150Val) | ClinVar dbSNP |
| 12 | g.13753879T>G | CA384054820 | GRIN2B | c.448A>C (p.Ile150Leu) | |
| 12 | g.13753879T= | CA2017525994 | GRIN2B | c.448A= (p.Ile150=) | |
| 12 | g.13753880T>A | CA478853541 | GRIN2B | c.447A>T (p.Ser149=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.13753880T>C | CA478853542 | GRIN2B | c.447A>G (p.Ser149=) | gnomAD v4 |
| 12 | g.13753880T>G | CA478853543 | GRIN2B | c.447A>C (p.Ser149=) | |
| 12 | g.13753880T= | CA2017525995 | GRIN2B | c.447A= (p.Ser149=) | |
| 12 | g.13753881G>A | CA384054822 | GRIN2B | c.446C>T (p.Ser149Leu) | |
| 12 | g.13753881G>C | CA384054824 | GRIN2B | c.446C>G (p.Ser149Ter) | |
| 12 | g.13753881G>T | CA384054825 | GRIN2B | c.446C>A (p.Ser149Ter) | |
| 12 | g.13753882A= | CA2017525996 | GRIN2B | c.445T= (p.Ser149=) | |
| 12 | g.13753882A>C | CA384054827 | GRIN2B | c.445T>G (p.Ser149Ala) | |
| 12 | g.13753882A>G | CA233116022 | GRIN2B | c.445T>C (p.Ser149Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 12 | g.13753882A>T | CA384054828 | GRIN2B | c.445T>A (p.Ser149Thr) | |
| 12 | g.13753883T>A | CA6461400 | GRIN2B | c.444A>T (p.Pro148=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.13753883T>C | CA6461399 | GRIN2B | c.444A>G (p.Pro148=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.13753883T>G | CA478853545 | GRIN2B | c.444A>C (p.Pro148=) | |
| 12 | g.13753883T= | CA2017525997 | GRIN2B | c.444A= (p.Pro148=) | |
| 12 | g.13753884G>A | CA384054831 | GRIN2B | c.443C>T (p.Pro148Leu) | |
| 12 | g.13753884G>C | CA384054833 | GRIN2B | c.443C>G (p.Pro148Arg) | |
| 12 | g.13753884G>T | CA384054834 | GRIN2B | c.443C>A (p.Pro148Gln) | |
| 12 | g.13753885G>A | CA384054836 | GRIN2B | c.442C>T (p.Pro148Ser) | COSMIC |
| 12 | g.13753885G>C | CA384054837 | GRIN2B | c.442C>G (p.Pro148Ala) | |
| 12 | g.13753885G>T | CA384054838 | GRIN2B | c.442C>A (p.Pro148Thr) | |
| 12 | g.13753886G>A | CA478853551 | GRIN2B | c.441C>T (p.Gly147=) | |
| 12 | g.13753886G>C | CA478853549 | GRIN2B | c.441C>G (p.Gly147=) | |
| 12 | g.13753886G>T | CA478853550 | GRIN2B | c.441C>A (p.Gly147=) | |
| 12 | g.13753887C>A | CA384054840 | GRIN2B | c.440G>T (p.Gly147Val) | |
| 12 | g.13753887C>G | CA384054841 | GRIN2B | c.440G>C (p.Gly147Ala) | |
| 12 | g.13753887C>T | CA384054843 | GRIN2B | c.440G>A (p.Gly147Asp) | gnomAD v4 COSMIC |
| 12 | g.13753888C>A | CA384054845 | GRIN2B | c.439G>T (p.Gly147Cys) | |
| 12 | g.13753888C>G | CA384054846 | GRIN2B | c.439G>C (p.Gly147Arg) | |
| 12 | g.13753888C>T | CA384054847 | GRIN2B | c.439G>A (p.Gly147Ser) | |
| 12 | g.13753889A>C | CA384054849 | GRIN2B | c.438T>G (p.Phe146Leu) | |
| 12 | g.13753889A>G | CA478853555 | GRIN2B | c.438T>C (p.Phe146=) | |
| 12 | g.13753889A>T | CA384054848 | GRIN2B | c.438T>A (p.Phe146Leu) | |
| 12 | g.13753890A>C | CA384054851 | GRIN2B | c.437T>G (p.Phe146Cys) | |
| 12 | g.13753890A>G | CA384054854 | GRIN2B | c.437T>C (p.Phe146Ser) | |
| 12 | g.13753890A>T | CA384054852 | GRIN2B | c.437T>A (p.Phe146Tyr) | |
| 12 | g.13753891A>C | CA384054855 | GRIN2B | c.436T>G (p.Phe146Val) | |
| 12 | g.13753891A>G | CA384054859 | GRIN2B | c.436T>C (p.Phe146Leu) | |
| 12 | g.13753891A>T | CA384054857 | GRIN2B | c.436T>A (p.Phe146Ile) | |
| 12 | g.13753892C>A | CA384054861 | GRIN2B | c.435G>T (p.Gln145His) | |
| 12 | g.13753892C>G | CA384054862 | GRIN2B | c.435G>C (p.Gln145His) | |
| 12 | g.13753892C>T | CA478853561 | GRIN2B | c.435G>A (p.Gln145=) | |
| 12 | g.13753893T>A | CA384054864 | GRIN2B | c.434A>T (p.Gln145Leu) | |
| 12 | g.13753893T>C | CA384054866 | GRIN2B | c.434A>G (p.Gln145Arg) | |
| 12 | g.13753893T>G | CA384054867 | GRIN2B | c.434A>C (p.Gln145Pro) | |
| 12 | g.13753894G>A | CA384054868 | GRIN2B | c.433C>T (p.Gln145Ter) | dbSNP |