Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
12 | g.13753894G>C | CA384054869 | GRIN2B | c.433C>G (p.Gln145Glu) | |
12 | g.13753894G= | CA2017525998 | GRIN2B | c.433C= (p.Gln145=) | |
12 | g.13753894G>T | CA384054870 | GRIN2B | c.433C>A (p.Gln145Lys) | |
12 | g.13753895G>A | CA478853566 | GRIN2B | c.432C>T (p.Phe144=) | |
12 | g.13753895G>C | CA384054871 | GRIN2B | c.432C>G (p.Phe144Leu) | |
12 | g.13753895G>T | CA384054872 | GRIN2B | c.432C>A (p.Phe144Leu) | COSMIC |
12 | g.13753896A>C | CA384054874 | GRIN2B | c.431T>G (p.Phe144Cys) | |
12 | g.13753896A>G | CA384054876 | GRIN2B | c.431T>C (p.Phe144Ser) | gnomAD v4 |
12 | g.13753896A>T | CA384054879 | GRIN2B | c.431T>A (p.Phe144Tyr) | |
12 | g.13753897A>C | CA384054884 | GRIN2B | c.430T>G (p.Phe144Val) | |
12 | g.13753897A>G | CA384054883 | GRIN2B | c.430T>C (p.Phe144Leu) | gnomAD v4 |
12 | g.13753897A>T | CA384054882 | GRIN2B | c.430T>A (p.Phe144Ile) | |
12 | g.13753898G>A | CA233116023 | GRIN2B | c.429C>T (p.Phe143=) | ClinVar dbSNP gnomAD v4 |
12 | g.13753898G>C | CA384054888 | GRIN2B | c.429C>G (p.Phe143Leu) | |
12 | g.13753898G= | CA2017525999 | GRIN2B | c.429C= (p.Phe143=) | |
12 | g.13753898G>T | CA384054889 | GRIN2B | c.429C>A (p.Phe143Leu) | gnomAD v4 COSMIC |
12 | g.13753899A>C | CA384054891 | GRIN2B | c.428T>G (p.Phe143Cys) | |
12 | g.13753899A>G | CA384054893 | GRIN2B | c.428T>C (p.Phe143Ser) | |
12 | g.13753899A>T | CA384054895 | GRIN2B | c.428T>A (p.Phe143Tyr) | |
12 | g.13753900A= | CA2017526000 | GRIN2B | c.427T= (p.Phe143=) | |
12 | g.13753900A>C | CA384054896 | GRIN2B | c.427T>G (p.Phe143Val) | |
12 | g.13753900A>G | CA6461401 | GRIN2B | c.427T>C (p.Phe143Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753900A>T | CA6461402 | GRIN2B | c.427T>A (p.Phe143Ile) | dbSNP ExAC gnomAD v2 |
12 | g.13753901C>A | CA384054900 | GRIN2B | c.426G>T (p.Met142Ile) | |
12 | g.13753901C= | CA2017526001 | GRIN2B | c.426G= (p.Met142=) |