Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.13753426T>A | CA384053190 | GRIN2B | c.901A>T (p.Thr301Ser) | |
12 | g.13753426T>C | CA384053191 | GRIN2B | c.901A>G (p.Thr301Ala) | |
12 | g.13753426T>G | CA384053192 | GRIN2B | c.901A>C (p.Thr301Pro) | |
12 | g.13753427G>A | CA478853480 | GRIN2B | c.900C>T (p.Ile300=) | dbSNP |
12 | g.13753427G>C | CA384053193 | GRIN2B | c.900C>G (p.Ile300Met) | |
12 | g.13753427G= | CA2017525828 | GRIN2B | c.900C= (p.Ile300=) | |
12 | g.13753427G>T | CA478853481 | GRIN2B | c.900C>A (p.Ile300=) | |
12 | g.13753428A>C | CA384053194 | GRIN2B | c.899T>G (p.Ile300Ser) | |
12 | g.13753428A>G | CA384053196 | GRIN2B | c.899T>C (p.Ile300Thr) | |
12 | g.13753428A>T | CA384053195 | GRIN2B | c.899T>A (p.Ile300Asn) | |
12 | g.13753429T>A | CA384053197 | GRIN2B | c.898A>T (p.Ile300Phe) | |
12 | g.13753429T>C | CA384053198 | GRIN2B | c.898A>G (p.Ile300Val) | |
12 | g.13753429T>G | CA384053199 | GRIN2B | c.898A>C (p.Ile300Leu) | |
12 | g.13753430T>A | CA478853486 | GRIN2B | c.897A>T (p.Ile299=) | |
12 | g.13753430T>C | CA384053200 | GRIN2B | c.897A>G (p.Ile299Met) | |
12 | g.13753430T>G | CA478853485 | GRIN2B | c.897A>C (p.Ile299=) | |
12 | g.13753431A>C | CA384053201 | GRIN2B | c.896T>G (p.Ile299Arg) | |
12 | g.13753431A>G | CA384053202 | GRIN2B | c.896T>C (p.Ile299Thr) | |
12 | g.13753431A>T | CA384053203 | GRIN2B | c.896T>A (p.Ile299Lys) | COSMIC |
12 | g.13753432T>A | CA384053204 | GRIN2B | c.895A>T (p.Ile299Leu) | |
12 | g.13753432T>C | CA6461353 | GRIN2B | c.895A>G (p.Ile299Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.13753432T>G | CA384053205 | GRIN2B | c.895A>C (p.Ile299Leu) | |
12 | g.13753432T= | CA2017525829 | GRIN2B | c.895A= (p.Ile299=) | |
12 | g.13753433G>A | CA478853487 | GRIN2B | c.894C>T (p.Ala298=) | |
12 | g.13753433G>C | CA478853488 | GRIN2B | c.894C>G (p.Ala298=) | |
12 | g.13753433G>T | CA478853489 | GRIN2B | c.894C>A (p.Ala298=) | |
12 | g.13753434G>A | CA384053206 | GRIN2B | c.893C>T (p.Ala298Val) | COSMIC |
12 | g.13753434G>C | CA384053207 | GRIN2B | c.893C>G (p.Ala298Gly) | |
12 | g.13753434G>T | CA384053208 | GRIN2B | c.893C>A (p.Ala298Asp) | gnomAD v4 |
12 | g.13753435C>A | CA384053209 | GRIN2B | c.892G>T (p.Ala298Ser) | |
12 | g.13753435C>G | CA384053211 | GRIN2B | c.892G>C (p.Ala298Pro) | |
12 | g.13753435C>T | CA384053210 | GRIN2B | c.892G>A (p.Ala298Thr) | |
12 | g.13753436A>C | CA384053212 | GRIN2B | c.891T>G (p.Ile297Met) | |
12 | g.13753436A>G | CA478853491 | GRIN2B | c.891T>C (p.Ile297=) | |
12 | g.13753436A>T | CA478853492 | GRIN2B | c.891T>A (p.Ile297=) | |
12 | g.13753437A>C | CA384053213 | GRIN2B | c.890T>G (p.Ile297Ser) | |
12 | g.13753437A>G | CA384053214 | GRIN2B | c.890T>C (p.Ile297Thr) | |
12 | g.13753437A>T | CA384053215 | GRIN2B | c.890T>A (p.Ile297Asn) | |
12 | g.13753438T>A | CA384053216 | GRIN2B | c.889A>T (p.Ile297Phe) | |
12 | g.13753438T>C | CA384053217 | GRIN2B | c.889A>G (p.Ile297Val) | |
12 | g.13753438T>G | CA384053218 | GRIN2B | c.889A>C (p.Ile297Leu) | |
12 | g.13753439T>A | CA478853493 | GRIN2B | c.888A>T (p.Gly296=) | |
12 | g.13753439T>C | CA478853495 | GRIN2B | c.888A>G (p.Gly296=) | |
12 | g.13753439T>G | CA478853494 | GRIN2B | c.888A>C (p.Gly296=) | gnomAD v4 |
12 | g.13753440C>A | CA384053219 | GRIN2B | c.887G>T (p.Gly296Val) | |
12 | g.13753440C>G | CA384053220 | GRIN2B | c.887G>C (p.Gly296Ala) | |
12 | g.13753440C>T | CA384053221 | GRIN2B | c.887G>A (p.Gly296Glu) | |
12 | g.13753441C>A | CA384053223 | GRIN2B | c.886G>T (p.Gly296Ter) | dbSNP |
12 | g.13753441C= | CA2017525830 | GRIN2B | c.886G= (p.Gly296=) | |
12 | g.13753441C>G | CA384053224 | GRIN2B | c.886G>C (p.Gly296Arg) |