Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13753686G>A | CA384054032 | GRIN2B | c.641C>T (p.Ser214Phe) | |
12 | g.13753686G>C | CA384054034 | GRIN2B | c.641C>G (p.Ser214Cys) | |
12 | g.13753686G>T | CA384054035 | GRIN2B | c.641C>A (p.Ser214Tyr) | |
12 | g.13753687A>C | CA384054037 | GRIN2B | c.640T>G (p.Ser214Ala) | |
12 | g.13753687A>G | CA384054038 | GRIN2B | c.640T>C (p.Ser214Pro) | |
12 | g.13753687A>T | CA384054040 | GRIN2B | c.640T>A (p.Ser214Thr) | |
12 | g.13753688A>C | CA384054042 | GRIN2B | c.639T>G (p.Asp213Glu) | gnomAD v4 |
12 | g.13753688A>G | CA478853703 | GRIN2B | c.639T>C (p.Asp213=) | |
12 | g.13753688A>T | CA384054043 | GRIN2B | c.639T>A (p.Asp213Glu) | |
12 | g.13753689T>A | CA384054045 | GRIN2B | c.638A>T (p.Asp213Val) | |
12 | g.13753689T>C | CA384054047 | GRIN2B | c.638A>G (p.Asp213Gly) | |
12 | g.13753689T>G | CA384054048 | GRIN2B | c.638A>C (p.Asp213Ala) | |
12 | g.13753690C>A | CA384054050 | GRIN2B | c.637G>T (p.Asp213Tyr) | |
12 | g.13753690C>G | CA384054051 | GRIN2B | c.637G>C (p.Asp213His) | |
12 | g.13753690C>T | CA384054052 | GRIN2B | c.637G>A (p.Asp213Asn) | |
12 | g.13753691T>A | CA478853706 | GRIN2B | c.636A>T (p.Gly212=) | |
12 | g.13753691T>C | CA478853710 | GRIN2B | c.636A>G (p.Gly212=) | |
12 | g.13753691T>G | CA478853708 | GRIN2B | c.636A>C (p.Gly212=) | |
12 | g.13753692C>A | CA384054055 | GRIN2B | c.635G>T (p.Gly212Val) | |
12 | g.13753692C>G | CA384054054 | GRIN2B | c.635G>C (p.Gly212Ala) | |
12 | g.13753692C>T | CA384054053 | GRIN2B | c.635G>A (p.Gly212Glu) | COSMIC |
12 | g.13753693C>A | CA384054056 | GRIN2B | c.634G>T (p.Gly212Ter) | |
12 | g.13753693C>G | CA384054057 | GRIN2B | c.634G>C (p.Gly212Arg) | |
12 | g.13753693C>T | CA384054058 | GRIN2B | c.634G>A (p.Gly212Arg) | COSMIC |
12 | g.13753694A= | CA2017525928 | GRIN2B | c.633T= (p.Asp211=) | |
12 | g.13753694A>C | CA384054059 | GRIN2B | c.633T>G (p.Asp211Glu) | |
12 | g.13753694A>G | CA478853713 | GRIN2B | c.633T>C (p.Asp211=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.13753694A>T | CA384054060 | GRIN2B | c.633T>A (p.Asp211Glu) | |
12 | g.13753695T>A | CA384054062 | GRIN2B | c.632A>T (p.Asp211Val) | |
12 | g.13753695T>C | CA384054064 | GRIN2B | c.632A>G (p.Asp211Gly) | |
12 | g.13753695T>G | CA384054065 | GRIN2B | c.632A>C (p.Asp211Ala) | |
12 | g.13753696C>A | CA384054066 | GRIN2B | c.631G>T (p.Asp211Tyr) | |
12 | g.13753696C= | CA2017525929 | GRIN2B | c.631G= (p.Asp211=) | |
12 | g.13753696C>G | CA384054067 | GRIN2B | c.631G>C (p.Asp211His) | |
12 | g.13753696C>T | CA384054069 | GRIN2B | c.631G>A (p.Asp211Asn) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.13753697G>A | CA6461381 | GRIN2B | c.630C>T (p.Asp210=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.13753697G>C | CA384054072 | GRIN2B | c.630C>G (p.Asp210Glu) | |
12 | g.13753697G= | CA2017525930 | GRIN2B | c.630C= (p.Asp210=) | |
12 | g.13753697G>T | CA384054074 | GRIN2B | c.630C>A (p.Asp210Glu) | |
12 | g.13753698T>A | CA384054080 | GRIN2B | c.629A>T (p.Asp210Val) | |
12 | g.13753698T>C | CA384054078 | GRIN2B | c.629A>G (p.Asp210Gly) | |
12 | g.13753698T>G | CA384054076 | GRIN2B | c.629A>C (p.Asp210Ala) | |
12 | g.13753699C>A | CA384054082 | GRIN2B | c.628G>T (p.Asp210Tyr) | |
12 | g.13753699C>G | CA384054084 | GRIN2B | c.628G>C (p.Asp210His) | |
12 | g.13753699C>T | CA384054086 | GRIN2B | c.628G>A (p.Asp210Asn) | |
12 | g.13753700C>A | CA478853719 | GRIN2B | c.627G>T (p.Leu209=) | |
12 | g.13753700C>G | CA478853720 | GRIN2B | c.627G>C (p.Leu209=) | |
12 | g.13753700C>T | CA478853721 | GRIN2B | c.627G>A (p.Leu209=) | ClinVar |
12 | g.13753701A>C | CA384054088 | GRIN2B | c.626T>G (p.Leu209Arg) | gnomAD v4 |
12 | g.13753701A>G | CA384054090 | GRIN2B | c.626T>C (p.Leu209Pro) |