| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.48419722G>A | CA10590055 | GRIN2D | c.1999G>A (p.Val667Ile) | ClinVar dbSNP |
| 19 | g.48419722G>C | CA406698252 | GRIN2D | c.1999G>C (p.Val667Leu) | |
| 19 | g.48419722G= | CA2339887608 | GRIN2D | c.1999G= (p.Val667=) | |
| 19 | g.48419722G>T | CA406698250 | GRIN2D | c.1999G>T (p.Val667Phe) | |
| 19 | g.48419723T>A | CA406698253 | GRIN2D | c.2000T>A (p.Val667Asp) | |
| 19 | g.48419723T>C | CA406698254 | GRIN2D | c.2000T>C (p.Val667Ala) | |
| 19 | g.48419723T>G | CA406698255 | GRIN2D | c.2000T>G (p.Val667Gly) | |
| 19 | g.48419724C>A | CA508038144 | GRIN2D | c.2001C>A (p.Val667=) | |
| 19 | g.48419724C>G | CA508038145 | GRIN2D | c.2001C>G (p.Val667=) | |
| 19 | g.48419724C>T | CA508038146 | GRIN2D | c.2001C>T (p.Val667=) | |
| 19 | g.48419725A>C | CA406698256 | GRIN2D | c.2002A>C (p.Ile668Leu) | |
| 19 | g.48419725A>G | CA406698257 | GRIN2D | c.2002A>G (p.Ile668Val) | |
| 19 | g.48419725A>T | CA406698258 | GRIN2D | c.2002A>T (p.Ile668Phe) | |
| 19 | g.48419726T>A | CA406698259 | GRIN2D | c.2003T>A (p.Ile668Asn) | |
| 19 | g.48419726T>C | CA406698260 | GRIN2D | c.2003T>C (p.Ile668Thr) | |
| 19 | g.48419726T>G | CA406698261 | GRIN2D | c.2003T>G (p.Ile668Ser) | |
| 19 | g.48419727C>A | CA508038147 | GRIN2D | c.2004C>A (p.Ile668=) | |
| 19 | g.48419727C>G | CA406698262 | GRIN2D | c.2004C>G (p.Ile668Met) | |
| 19 | g.48419727C>T | CA508038148 | GRIN2D | c.2004C>T (p.Ile668=) | |
| 19 | g.48419728T>A | CA406698263 | GRIN2D | c.2005T>A (p.Phe669Ile) | |
| 19 | g.48419728T>C | CA406698264 | GRIN2D | c.2005T>C (p.Phe669Leu) | |
| 19 | g.48419728T>G | CA406698265 | GRIN2D | c.2005T>G (p.Phe669Val) | COSMIC |
| 19 | g.48419729T>A | CA406698268 | GRIN2D | c.2006T>A (p.Phe669Tyr) | |
| 19 | g.48419729T>C | CA406698266 | GRIN2D | c.2006T>C (p.Phe669Ser) | |
| 19 | g.48419729T>G | CA406698267 | GRIN2D | c.2006T>G (p.Phe669Cys) | |
| 19 | g.48419730C>A | CA406698269 | GRIN2D | c.2007C>A (p.Phe669Leu) | |
| 19 | g.48419730C>G | CA406698270 | GRIN2D | c.2007C>G (p.Phe669Leu) | |
| 19 | g.48419730C>T | CA508038149 | GRIN2D | c.2007C>T (p.Phe669=) | |
| 19 | g.48419731C>A | CA406698271 | GRIN2D | c.2008C>A (p.Leu670Ile) | |
| 19 | g.48419731C= | CA2339887609 | GRIN2D | c.2008C= (p.Leu670=) | |
| 19 | g.48419731C>G | CA406698272 | GRIN2D | c.2008C>G (p.Leu670Val) | |
| 19 | g.48419731C>T | CA406698273 | GRIN2D | c.2008C>T (p.Leu670Phe) | ClinVar |
| 19 | g.48419732T>A | CA406698274 | GRIN2D | c.2009T>A (p.Leu670His) | |
| 19 | g.48419732T>C | CA406698275 | GRIN2D | c.2009T>C (p.Leu670Pro) | |
| 19 | g.48419732T>G | CA406698276 | GRIN2D | c.2009T>G (p.Leu670Arg) | |
| 19 | g.48419733C>A | CA508038150 | GRIN2D | c.2010C>A (p.Leu670=) | |
| 19 | g.48419733C= | CA2339887610 | GRIN2D | c.2010C= (p.Leu670=) | |
| 19 | g.48419733C>G | CA508038151 | GRIN2D | c.2010C>G (p.Leu670=) | |
| 19 | g.48419733C>T | CA9550634 | GRIN2D | c.2010C>T (p.Leu670=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.48419734G>A | CA406698277 | GRIN2D | c.2011G>A (p.Ala671Thr) | dbSNP |
| 19 | g.48419734G>C | CA406698278 | GRIN2D | c.2011G>C (p.Ala671Pro) | |
| 19 | g.48419734G= | CA2339887611 | GRIN2D | c.2011G= (p.Ala671=) | |
| 19 | g.48419734G>T | CA406698279 | GRIN2D | c.2011G>T (p.Ala671Ser) | |
| 19 | g.48419735C>A | CA406698281 | GRIN2D | c.2012C>A (p.Ala671Asp) | |
| 19 | g.48419735C>G | CA406698282 | GRIN2D | c.2012C>G (p.Ala671Gly) | |
| 19 | g.48419735C>T | CA406698280 | GRIN2D | c.2012C>T (p.Ala671Val) | |
| 19 | g.48419736C>A | CA508038152 | GRIN2D | c.2013C>A (p.Ala671=) | |
| 19 | g.48419736C= | CA2339887612 | GRIN2D | c.2013C= (p.Ala671=) | |
| 19 | g.48419736C>G | CA9550635 | GRIN2D | c.2013C>G (p.Ala671=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 19 | g.48419736C>T | CA508038153 | GRIN2D | c.2013C>T (p.Ala671=) |