Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.48419710G>A | CA406698199 | GRIN2D | c.1987G>A (p.Ala663Thr) | |
19 | g.48419710G>C | CA406698198 | GRIN2D | c.1987G>C (p.Ala663Pro) | |
19 | g.48419710G>T | CA406698196 | GRIN2D | c.1987G>T (p.Ala663Ser) | gnomAD v4 |
19 | g.48419711C>A | CA406698202 | GRIN2D | c.1988C>A (p.Ala663Asp) | |
19 | g.48419711C>G | CA406698205 | GRIN2D | c.1988C>G (p.Ala663Gly) | |
19 | g.48419711C>T | CA406698204 | GRIN2D | c.1988C>T (p.Ala663Val) | |
19 | g.48419712C>A | CA9550631 | GRIN2D | c.1989C>A (p.Ala663=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48419712C= | CA2339887605 | GRIN2D | c.1989C= (p.Ala663=) | |
19 | g.48419712C>G | CA508038140 | GRIN2D | c.1989C>G (p.Ala663=) | |
19 | g.48419712C>T | CA508038139 | GRIN2D | c.1989C>T (p.Ala663=) | |
19 | g.48419713T>A | CA406698210 | GRIN2D | c.1990T>A (p.Phe664Ile) | |
19 | g.48419713T>C | CA406698212 | GRIN2D | c.1990T>C (p.Phe664Leu) | |
19 | g.48419713T>G | CA406698213 | GRIN2D | c.1990T>G (p.Phe664Val) | |
19 | g.48419714T>A | CA406698216 | GRIN2D | c.1991T>A (p.Phe664Tyr) | |
19 | g.48419714T>C | CA406698218 | GRIN2D | c.1991T>C (p.Phe664Ser) | |
19 | g.48419714T>G | CA406698220 | GRIN2D | c.1991T>G (p.Phe664Cys) | ClinVar |
19 | g.48419715C>A | CA406698223 | GRIN2D | c.1992C>A (p.Phe664Leu) | |
19 | g.48419715C>G | CA406698224 | GRIN2D | c.1992C>G (p.Phe664Leu) | |
19 | g.48419715C>T | CA508038141 | GRIN2D | c.1992C>T (p.Phe664=) | gnomAD v4 |
19 | g.48419716T>A | CA406698226 | GRIN2D | c.1993T>A (p.Phe665Ile) | |
19 | g.48419716T>C | CA406698228 | GRIN2D | c.1993T>C (p.Phe665Leu) | |
19 | g.48419716T>G | CA406698230 | GRIN2D | c.1993T>G (p.Phe665Val) | |
19 | g.48419717T>A | CA406698234 | GRIN2D | c.1994T>A (p.Phe665Tyr) | |
19 | g.48419717T>C | CA406698231 | GRIN2D | c.1994T>C (p.Phe665Ser) | dbSNP |
19 | g.48419717T>G | CA406698232 | GRIN2D | c.1994T>G (p.Phe665Cys) | |
19 | g.48419718C>A | CA406698236 | GRIN2D | c.1995C>A (p.Phe665Leu) | |
19 | g.48419718C= | CA2339887606 | GRIN2D | c.1995C= (p.Phe665=) | |
19 | g.48419718C>G | CA406698238 | GRIN2D | c.1995C>G (p.Phe665Leu) | |
19 | g.48419718C>T | CA9550632 | GRIN2D | c.1995C>T (p.Phe665=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.48419719G>A | CA406698239 | GRIN2D | c.1996G>A (p.Ala666Thr) | |
19 | g.48419719G>C | CA406698241 | GRIN2D | c.1996G>C (p.Ala666Pro) | |
19 | g.48419719G>T | CA406698243 | GRIN2D | c.1996G>T (p.Ala666Ser) | |
19 | g.48419720C>A | CA406698245 | GRIN2D | c.1997C>A (p.Ala666Asp) | |
19 | g.48419720C>G | CA406698246 | GRIN2D | c.1997C>G (p.Ala666Gly) | |
19 | g.48419720C>T | CA406698247 | GRIN2D | c.1997C>T (p.Ala666Val) | ClinVar dbSNP COSMIC |
19 | g.48419721C>A | CA508038143 | GRIN2D | c.1998C>A (p.Ala666=) | |
19 | g.48419721C= | CA2339887607 | GRIN2D | c.1998C= (p.Ala666=) | |
19 | g.48419721C>G | CA508038142 | GRIN2D | c.1998C>G (p.Ala666=) | |
19 | g.48419721C>T | CA9550633 | GRIN2D | c.1998C>T (p.Ala666=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
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.48419723_48419724del | CA2814653934 | GRIN2D | c.2000_2001del (p.Val667AspfsTer28) | |
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=) | |
19 | g.48419737A>C | CA406698283 | GRIN2D | c.2014A>C (p.Ser672Arg) | |
19 | g.48419737A>G | CA406698285 | GRIN2D | c.2014A>G (p.Ser672Gly) | |
19 | g.48419737A>T | CA406698284 | GRIN2D | c.2014A>T (p.Ser672Cys) | |
19 | g.48419738G>A | CA406698286 | GRIN2D | c.2015G>A (p.Ser672Asn) | |
19 | g.48419738G>C | CA309338912 | GRIN2D | c.2015G>C (p.Ser672Thr) | dbSNP |
19 | g.48419738G= | CA2339887613 | GRIN2D | c.2015G= (p.Ser672=) | |
19 | g.48419738G>T | CA406698287 | GRIN2D | c.2015G>T (p.Ser672Ile) | |
19 | g.48419739C>A | CA406698288 | GRIN2D | c.2016C>A (p.Ser672Arg) | |
19 | g.48419739C>G | CA406698289 | GRIN2D | c.2016C>G (p.Ser672Arg) | |
19 | g.48419739C>T | CA508038154 | GRIN2D | c.2016C>T (p.Ser672=) | |
19 | g.48419740T>A | CA406698290 | GRIN2D | c.2017T>A (p.Tyr673Asn) | |
19 | g.48419740T>C | CA406698291 | GRIN2D | c.2017T>C (p.Tyr673His) | |
19 | g.48419740T>G | CA406698292 | GRIN2D | c.2017T>G (p.Tyr673Asp) | |
19 | g.48419741A>C | CA406698293 | GRIN2D | c.2018A>C (p.Tyr673Ser) | |
19 | g.48419741A>G | CA406698294 | GRIN2D | c.2018A>G (p.Tyr673Cys) | |
19 | g.48419741A>T | CA406698295 | GRIN2D | c.2018A>T (p.Tyr673Phe) | |
19 | g.48419742C>A | CA406698297 | GRIN2D | c.2019C>A (p.Tyr673Ter) | |
19 | g.48419742C= | CA2339887614 | GRIN2D | c.2019C= (p.Tyr673=) | |
19 | g.48419742C>G | CA406698296 | GRIN2D | c.2019C>G (p.Tyr673Ter) | |
19 | g.48419742C>T | CA9550636 | GRIN2D | c.2019C>T (p.Tyr673=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48419743A>C | CA406698298 | GRIN2D | c.2020A>C (p.Thr674Pro) | |
19 | g.48419743A>G | CA406698299 | GRIN2D | c.2020A>G (p.Thr674Ala) | |
19 | g.48419743A>T | CA406698300 | GRIN2D | c.2020A>T (p.Thr674Ser) | |
19 | g.48419744C>A | CA406698301 | GRIN2D | c.2021C>A (p.Thr674Lys) | |
19 | g.48419744C>G | CA406698302 | GRIN2D | c.2021C>G (p.Thr674Arg) | |
19 | g.48419744C>T | CA406698303 | GRIN2D | c.2021C>T (p.Thr674Ile) | gnomAD v4 |
19 | g.48419745A>C | CA508038155 | GRIN2D | c.2022A>C (p.Thr674=) | |
19 | g.48419745A>G | CA508038156 | GRIN2D | c.2022A>G (p.Thr674=) | gnomAD v4 |
19 | g.48419745A>T | CA508038157 | GRIN2D | c.2022A>T (p.Thr674=) | |
19 | g.48419746G>A | CA406698304 | GRIN2D | c.2023G>A (p.Ala675Thr) | ClinVar dbSNP |
19 | g.48419746G>C | CA406698305 | GRIN2D | c.2023G>C (p.Ala675Pro) | ClinVar dbSNP |
19 | g.48419746G= | CA2339887615 | GRIN2D | c.2023G= (p.Ala675=) | |
19 | g.48419746G>T | CA406698306 | GRIN2D | c.2023G>T (p.Ala675Ser) | |
19 | g.48419747C>A | CA406698307 | GRIN2D | c.2024C>A (p.Ala675Asp) | ClinVar dbSNP |
19 | g.48419747C= | CA2339887616 | GRIN2D | c.2024C= (p.Ala675=) | |
19 | g.48419747C>G | CA406698308 | GRIN2D | c.2024C>G (p.Ala675Gly) | |
19 | g.48419747C>T | CA406698309 | GRIN2D | c.2024C>T (p.Ala675Val) | ClinVar dbSNP |
19 | g.48419748C>A | CA508038158 | GRIN2D | c.2025C>A (p.Ala675=) | |
19 | g.48419748C= | CA2339887617 | GRIN2D | c.2025C= (p.Ala675=) | |
19 | g.48419748C>G | CA508038159 | GRIN2D | c.2025C>G (p.Ala675=) | |
19 | g.48419748C>T | CA508038160 | GRIN2D | c.2025C>T (p.Ala675=) | dbSNP |
19 | g.48419749A>C | CA406698312 | GRIN2D | c.2026A>C (p.Asn676His) | |
19 | g.48419749A>G | CA406698311 | GRIN2D | c.2026A>G (p.Asn676Asp) | |
19 | g.48419749A>T | CA406698310 | GRIN2D | c.2026A>T (p.Asn676Tyr) | |
19 | g.48419750A>C | CA406698313 | GRIN2D | c.2027A>C (p.Asn676Thr) | |
19 | g.48419750A>G | CA406698314 | GRIN2D | c.2027A>G (p.Asn676Ser) | |
19 | g.48419750A>T | CA406698315 | GRIN2D | c.2027A>T (p.Asn676Ile) | ClinVar |
19 | g.48419751C>A | CA406698316 | GRIN2D | c.2028C>A (p.Asn676Lys) | gnomAD v4 |
19 | g.48419751C= | CA2339887618 | GRIN2D | c.2028C= (p.Asn676=) | |
19 | g.48419751C>G | CA406698317 | GRIN2D | c.2028C>G (p.Asn676Lys) | |
19 | g.48419751C>T | CA508038161 | GRIN2D | c.2028C>T (p.Asn676=) | dbSNP gnomAD v4 |
19 | g.48419752C>A | CA406698318 | GRIN2D | c.2029C>A (p.Leu677Met) | |
19 | g.48419752C= | CA2339887619 | GRIN2D | c.2029C= (p.Leu677=) | |
19 | g.48419752C>G | CA406698319 | GRIN2D | c.2029C>G (p.Leu677Val) | ClinVar dbSNP |
19 | g.48419752C>T | CA309338917 | GRIN2D | c.2029C>T (p.Leu677=) | dbSNP |
19 | g.48419753T>A | CA406698320 | GRIN2D | c.2030T>A (p.Leu677Gln) | |
19 | g.48419753T>C | CA406698322 | GRIN2D | c.2030T>C (p.Leu677Pro) | |
19 | g.48419753T>G | CA406698321 | GRIN2D | c.2030T>G (p.Leu677Arg) | |
19 | g.48419754G>A | CA9550637 | GRIN2D | c.2031G>A (p.Leu677=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48419754G>C | CA508038162 | GRIN2D | c.2031G>C (p.Leu677=) | gnomAD v4 |
19 | g.48419754G= | CA2339887620 | GRIN2D | c.2031G= (p.Leu677=) | |
19 | g.48419754G>T | CA508038163 | GRIN2D | c.2031G>T (p.Leu677=) | |
19 | g.48419755G>A | CA406698323 | GRIN2D | c.2032G>A (p.Ala678Thr) | |
19 | g.48419755G>C | CA406698324 | GRIN2D | c.2032G>C (p.Ala678Pro) | |
19 | g.48419755G>T | CA406698325 | GRIN2D | c.2032G>T (p.Ala678Ser) | |
19 | g.48419756C>A | CA406698326 | GRIN2D | c.2033C>A (p.Ala678Asp) | ClinVar dbSNP |
19 | g.48419756C>G | CA406698328 | GRIN2D | c.2033C>G (p.Ala678Gly) | |
19 | g.48419756C>T | CA406698327 | GRIN2D | c.2033C>T (p.Ala678Val) | |
19 | g.48419757C>A | CA508038164 | GRIN2D | c.2034C>A (p.Ala678=) | |
19 | g.48419757C= | CA2339887621 | GRIN2D | c.2034C= (p.Ala678=) | |
19 | g.48419757C>G | CA508038165 | GRIN2D | c.2034C>G (p.Ala678=) | dbSNP |
19 | g.48419757C>T | CA508038166 | GRIN2D | c.2034C>T (p.Ala678=) | |
19 | g.48419758G>A | CA406698329 | GRIN2D | c.2035G>A (p.Ala679Thr) | gnomAD v4 |
19 | g.48419758G>C | CA406698330 | GRIN2D | c.2035G>C (p.Ala679Pro) | |
19 | g.48419758G= | CA2339887622 | GRIN2D | c.2035G= (p.Ala679=) | |
19 | g.48419758G>T | CA406698331 | GRIN2D | c.2035G>T (p.Ala679Ser) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48419759C>A | CA406698332 | GRIN2D | c.2036C>A (p.Ala679Asp) | |
19 | g.48419759C>G | CA406698333 | GRIN2D | c.2036C>G (p.Ala679Gly) | |
19 | g.48419759C>T | CA406698334 | GRIN2D | c.2036C>T (p.Ala679Val) | |
19 | g.48419760C>A | CA508038167 | GRIN2D | c.2037C>A (p.Ala679=) | |
19 | g.48419760C= | CA2339887623 | GRIN2D | c.2037C= (p.Ala679=) | |
19 | g.48419760C>G | CA508038168 | GRIN2D | c.2037C>G (p.Ala679=) | |
19 | g.48419760C>T | CA508038169 | GRIN2D | c.2037C>T (p.Ala679=) | dbSNP gnomAD v2 |
19 | g.48419761T>A | CA406698335 | GRIN2D | c.2038T>A (p.Phe680Ile) | |
19 | g.48419761T>C | CA406698336 | GRIN2D | c.2038T>C (p.Phe680Leu) | gnomAD v4 |
19 | g.48419761T>G | CA406698337 | GRIN2D | c.2038T>G (p.Phe680Val) | |
19 | g.48419762T>A | CA406698338 | GRIN2D | c.2039T>A (p.Phe680Tyr) | |
19 | g.48419762T>C | CA406698339 | GRIN2D | c.2039T>C (p.Phe680Ser) | |
19 | g.48419762T>G | CA406698340 | GRIN2D | c.2039T>G (p.Phe680Cys) | |
19 | g.48419763C>A | CA406698341 | GRIN2D | c.2040C>A (p.Phe680Leu) | |
19 | g.48419763C>G | CA406698342 | GRIN2D | c.2040C>G (p.Phe680Leu) | |
19 | g.48419763C>T | CA508038170 | GRIN2D | c.2040C>T (p.Phe680=) | |
19 | g.48419764A= | CA2339887624 | GRIN2D | c.2041A= (p.Met681=) | |
19 | g.48419764A>C | CA406698343 | GRIN2D | c.2041A>C (p.Met681Leu) | ClinVar dbSNP |
19 | g.48419764A>G | CA406698345 | GRIN2D | c.2041A>G (p.Met681Val) | ClinVar dbSNP |
19 | g.48419764A>T | CA406698344 | GRIN2D | c.2041A>T (p.Met681Leu) | |
19 | g.48419765T>A | CA406698346 | GRIN2D | c.2042T>A (p.Met681Lys) | |
19 | g.48419765T>C | CA406698347 | GRIN2D | c.2042T>C (p.Met681Thr) | |
19 | g.48419765T>G | CA406698348 | GRIN2D | c.2042T>G (p.Met681Arg) | |
19 | g.48419766G>A | CA406698349 | GRIN2D | c.2043G>A (p.Met681Ile) | |
19 | g.48419766G>C | CA406698350 | GRIN2D | c.2043G>C (p.Met681Ile) | ClinVar dbSNP |
19 | g.48419766G= | CA2339887625 | GRIN2D | c.2043G= (p.Met681=) | |
19 | g.48419766G>T | CA406698351 | GRIN2D | c.2043G>T (p.Met681Ile) | |
19 | g.48419767A>C | CA406698352 | GRIN2D | c.2044A>C (p.Ile682Leu) | |
19 | g.48419767A>G | CA406698353 | GRIN2D | c.2044A>G (p.Ile682Val) | |
19 | g.48419767A>T | CA406698354 | GRIN2D | c.2044A>T (p.Ile682Phe) | |
19 | g.48419768T>A | CA406698355 | GRIN2D | c.2045T>A (p.Ile682Asn) | |
19 | g.48419768T>C | CA406698356 | GRIN2D | c.2045T>C (p.Ile682Thr) | |
19 | g.48419768T>G | CA406698357 | GRIN2D | c.2045T>G (p.Ile682Ser) | |
19 | g.48419769C>A | CA508038171 | GRIN2D | c.2046C>A (p.Ile682=) | |
19 | g.48419769C>G | CA406698358 | GRIN2D | c.2046C>G (p.Ile682Met) | |
19 | g.48419769C>T | CA508038172 | GRIN2D | c.2046C>T (p.Ile682=) | |
19 | g.48419770C>A | CA406698359 | GRIN2D | c.2047C>A (p.Gln683Lys) | |
19 | g.48419770C>G | CA406698361 | GRIN2D | c.2047C>G (p.Gln683Glu) | |
19 | g.48419770C>T | CA406698360 | GRIN2D | c.2047C>T (p.Gln683Ter) | |
19 | g.48419771A>C | CA406698362 | GRIN2D | c.2048A>C (p.Gln683Pro) | |
19 | g.48419771A>G | CA406698363 | GRIN2D | c.2048A>G (p.Gln683Arg) | |
19 | g.48419771A>T | CA406698364 | GRIN2D | c.2048A>T (p.Gln683Leu) | |
19 | g.48419772G>A | CA508038173 | GRIN2D | c.2049G>A (p.Gln683=) | |
19 | g.48419772G>C | CA406698365 | GRIN2D | c.2049G>C (p.Gln683His) | |
19 | g.48419772G>T | CA406698366 | GRIN2D | c.2049G>T (p.Gln683His) | |
19 | g.48419773G>A | CA406698367 | GRIN2D | c.2050G>A (p.Glu684Lys) | COSMIC |
19 | g.48419773G>C | CA406698368 | GRIN2D | c.2050G>C (p.Glu684Gln) | |
19 | g.48419773G>T | CA406698369 | GRIN2D | c.2050G>T (p.Glu684Ter) | |
19 | g.48419774A>C | CA406698370 | GRIN2D | c.2051A>C (p.Glu684Ala) | |
19 | g.48419774A>G | CA406698371 | GRIN2D | c.2051A>G (p.Glu684Gly) | |
19 | g.48419774A>T | CA406698372 | GRIN2D | c.2051A>T (p.Glu684Val) | |
19 | g.48419775G>A | CA508038174 | GRIN2D | c.2052G>A (p.Glu684=) | gnomAD v4 |
19 | g.48419775G>C | CA406698374 | GRIN2D | c.2052G>C (p.Glu684Asp) | |
19 | g.48419775G>T | CA406698373 | GRIN2D | c.2052G>T (p.Glu684Asp) | |
19 | g.48419776G>A | CA406698375 | GRIN2D | c.2053G>A (p.Glu685Lys) | |
19 | g.48419776G>C | CA406698376 | GRIN2D | c.2053G>C (p.Glu685Gln) | |
19 | g.48419776G>T | CA406698377 | GRIN2D | c.2053G>T (p.Glu685Ter) | |
19 | g.48419777A>C | CA406698378 | GRIN2D | c.2054A>C (p.Glu685Ala) | |
19 | g.48419777A>G | CA406698379 | GRIN2D | c.2054A>G (p.Glu685Gly) | |
19 | g.48419777A>T | CA406698380 | GRIN2D | c.2054A>T (p.Glu685Val) | |
19 | g.48419778G>A | CA508038175 | GRIN2D | c.2055G>A (p.Glu685=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48419778G>C | CA406698381 | GRIN2D | c.2055G>C (p.Glu685Asp) | |
19 | g.48419778G= | CA2339887626 | GRIN2D | c.2055G= (p.Glu685=) | |
19 | g.48419778G>T | CA406698382 | GRIN2D | c.2055G>T (p.Glu685Asp) | |
19 | g.48419779T>A | CA406698383 | GRIN2D | c.2056T>A (p.Tyr686Asn) | gnomAD v4 |
19 | g.48419779T>C | CA406698384 | GRIN2D | c.2056T>C (p.Tyr686His) | |
19 | g.48419779T>G | CA406698385 | GRIN2D | c.2056T>G (p.Tyr686Asp) | |
19 | g.48419780A>C | CA406698386 | GRIN2D | c.2057A>C (p.Tyr686Ser) | |
19 | g.48419780A>G | CA406698387 | GRIN2D | c.2057A>G (p.Tyr686Cys) | gnomAD v4 |
19 | g.48419780A>T | CA406698388 | GRIN2D | c.2057A>T (p.Tyr686Phe) | |
19 | g.48419781C>A | CA406698390 | GRIN2D | c.2058C>A (p.Tyr686Ter) | |
19 | g.48419781C>G | CA406698389 | GRIN2D | c.2058C>G (p.Tyr686Ter) | gnomAD v4 |
19 | g.48419781C>T | CA508038176 | GRIN2D | c.2058C>T (p.Tyr686=) | gnomAD v4 |
19 | g.48419782G>A | CA406698391 | GRIN2D | c.2059G>A (p.Val687Met) | gnomAD v4 |
19 | g.48419782G>C | CA406698392 | GRIN2D | c.2059G>C (p.Val687Leu) | |
19 | g.48419782G>T | CA406698393 | GRIN2D | c.2059G>T (p.Val687Leu) | |
19 | g.48419783T>A | CA406698394 | GRIN2D | c.2060T>A (p.Val687Glu) | |
19 | g.48419783T>C | CA406698395 | GRIN2D | c.2060T>C (p.Val687Ala) | |
19 | g.48419783T>G | CA406698396 | GRIN2D | c.2060T>G (p.Val687Gly) | |
19 | g.48419784G>A | CA508038177 | GRIN2D | c.2061G>A (p.Val687=) | gnomAD v4 |
19 | g.48419784G>C | CA508038178 | GRIN2D | c.2061G>C (p.Val687=) | |
19 | g.48419784G>T | CA508038179 | GRIN2D | c.2061G>T (p.Val687=) | |
19 | g.48419785G>A | CA406698397 | GRIN2D | c.2062G>A (p.Asp688Asn) | |
19 | g.48419785G>C | CA406698398 | GRIN2D | c.2062G>C (p.Asp688His) | gnomAD v4 |
19 | g.48419785G>T | CA406698399 | GRIN2D | c.2062G>T (p.Asp688Tyr) | |
19 | g.48419786A>C | CA406698400 | GRIN2D | c.2063A>C (p.Asp688Ala) | |
19 | g.48419786A>G | CA406698401 | GRIN2D | c.2063A>G (p.Asp688Gly) | |
19 | g.48419786A>T | CA406698402 | GRIN2D | c.2063A>T (p.Asp688Val) | |
19 | g.48419787T>A | CA406698403 | GRIN2D | c.2064T>A (p.Asp688Glu) | |
19 | g.48419787T>C | CA508038180 | GRIN2D | c.2064T>C (p.Asp688=) | |
19 | g.48419787T>G | CA406698404 | GRIN2D | c.2064T>G (p.Asp688Glu) | |
19 | g.48419788A>C | CA406698406 | GRIN2D | c.2065A>C (p.Thr689Pro) | |
19 | g.48419788A>G | CA406698407 | GRIN2D | c.2065A>G (p.Thr689Ala) | |
19 | g.48419788A>T | CA406698405 | GRIN2D | c.2065A>T (p.Thr689Ser) | |
19 | g.48419789C>A | CA406698409 | GRIN2D | c.2066C>A (p.Thr689Asn) | |
19 | g.48419789C>G | CA406698408 | GRIN2D | c.2066C>G (p.Thr689Ser) | |
19 | g.48419789C>T | CA406698410 | GRIN2D | c.2066C>T (p.Thr689Ile) | |
19 | g.48419790T>A | CA508038181 | GRIN2D | c.2067T>A (p.Thr689=) | |
19 | g.48419790T>C | CA508038183 | GRIN2D | c.2067T>C (p.Thr689=) | gnomAD v4 |
19 | g.48419790T>G | CA508038182 | GRIN2D | c.2067T>G (p.Thr689=) | ClinVar dbSNP |
19 | g.48419790T= | CA2339887627 | GRIN2D | c.2067T= (p.Thr689=) | |
19 | g.48419791G>A | CA406698411 | GRIN2D | c.2068G>A (p.Val690Met) | |
19 | g.48419791G>C | CA406698413 | GRIN2D | c.2068G>C (p.Val690Leu) | |
19 | g.48419791G>T | CA406698412 | GRIN2D | c.2068G>T (p.Val690Leu) | |
19 | g.48419792T>A | CA406698414 | GRIN2D | c.2069T>A (p.Val690Glu) | gnomAD v4 |
19 | g.48419792T>C | CA406698415 | GRIN2D | c.2069T>C (p.Val690Ala) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48419792T>G | CA406698416 | GRIN2D | c.2069T>G (p.Val690Gly) | |
19 | g.48419792T= | CA2339887628 | GRIN2D | c.2069T= (p.Val690=) | |
19 | g.48419793G>A | CA508038184 | GRIN2D | c.2070G>A (p.Val690=) | |
19 | g.48419793G>C | CA508038185 | GRIN2D | c.2070G>C (p.Val690=) | |
19 | g.48419793G>T | CA508038186 | GRIN2D | c.2070G>T (p.Val690=) | |
19 | g.48419794_48419831del | CA2586189621 | GRIN2D | c.2071_2091+17del | gnomAD v4 |
19 | g.48419794T>A | CA406698417 | GRIN2D | c.2071T>A (p.Ser691Thr) | |
19 | g.48419794T>C | CA406698418 | GRIN2D | c.2071T>C (p.Ser691Pro) | gnomAD v4 |
19 | g.48419794T>G | CA406698419 | GRIN2D | c.2071T>G (p.Ser691Ala) | |
19 | g.48419795C>A | CA406698422 | GRIN2D | c.2072C>A (p.Ser691Tyr) | |
19 | g.48419795C>G | CA406698421 | GRIN2D | c.2072C>G (p.Ser691Cys) | |
19 | g.48419795C>T | CA406698420 | GRIN2D | c.2072C>T (p.Ser691Phe) | COSMIC |
19 | g.48419796T>A | CA508038187 | GRIN2D | c.2073T>A (p.Ser691=) | |
19 | g.48419796T>C | CA508038188 | GRIN2D | c.2073T>C (p.Ser691=) | gnomAD v4 |
19 | g.48419796T>G | CA508038189 | GRIN2D | c.2073T>G (p.Ser691=) | |
19 | g.48419797G>A | CA406698423 | GRIN2D | c.2074G>A (p.Gly692Arg) | gnomAD v4 |
19 | g.48419797G>C | CA406698424 | GRIN2D | c.2074G>C (p.Gly692Arg) | |
19 | g.48419797G>T | CA406698425 | GRIN2D | c.2074G>T (p.Gly692Trp) | |
19 | g.48419798G>A | CA406698426 | GRIN2D | c.2075G>A (p.Gly692Glu) | |
19 | g.48419798G>C | CA406698427 | GRIN2D | c.2075G>C (p.Gly692Ala) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.48419798G= | CA2339887629 | GRIN2D | c.2075G= (p.Gly692=) | |
19 | g.48419798G>T | CA406698428 | GRIN2D | c.2075G>T (p.Gly692Val) | |
19 | g.48419799G>A | CA508038190 | GRIN2D | c.2076G>A (p.Gly692=) | gnomAD v4 |
19 | g.48419799G>C | CA508038191 | GRIN2D | c.2076G>C (p.Gly692=) | dbSNP |
19 | g.48419799G= | CA2339887630 | GRIN2D | c.2076G= (p.Gly692=) | |
19 | g.48419799G>T | CA508038192 | GRIN2D | c.2076G>T (p.Gly692=) | COSMIC |
19 | g.48419800C>A | CA406698429 | GRIN2D | c.2077C>A (p.Leu693Ile) | |
19 | g.48419800C>G | CA406698431 | GRIN2D | c.2077C>G (p.Leu693Val) | |
19 | g.48419800C>T | CA406698430 | GRIN2D | c.2077C>T (p.Leu693Phe) | |
19 | g.48419801T>A | CA406698432 | GRIN2D | c.2078T>A (p.Leu693His) | gnomAD v4 |
19 | g.48419801T>C | CA406698433 | GRIN2D | c.2078T>C (p.Leu693Pro) | |
19 | g.48419801T>G | CA406698434 | GRIN2D | c.2078T>G (p.Leu693Arg) | |
19 | g.48419802C>A | CA508038193 | GRIN2D | c.2079C>A (p.Leu693=) | |
19 | g.48419802C>G | CA508038194 | GRIN2D | c.2079C>G (p.Leu693=) | |
19 | g.48419802C>T | CA508038195 | GRIN2D | c.2079C>T (p.Leu693=) | gnomAD v4 |
19 | g.48419803A= | CA2339887631 | GRIN2D | c.2080A= (p.Ser694=) | |
19 | g.48419803A>C | CA406698435 | GRIN2D | c.2080A>C (p.Ser694Arg) | ClinVar dbSNP |
19 | g.48419803A>G | CA406698436 | GRIN2D | c.2080A>G (p.Ser694Gly) | |
19 | g.48419803A>T | CA406698437 | GRIN2D | c.2080A>T (p.Ser694Cys) | |
19 | g.48419803_48419804insCACACACCTTGCG | CA2814653949 | GRIN2D | c.2080_2081insCACACACCTTGCG (p.Ser694ThrfsTer6) | |
19 | g.48419804G>A | CA406698438 | GRIN2D | c.2081G>A (p.Ser694Asn) | |
19 | g.48419804G>C | CA406698439 | GRIN2D | c.2081G>C (p.Ser694Thr) | |
19 | g.48419804G>T | CA406698440 | GRIN2D | c.2081G>T (p.Ser694Ile) | |
19 | g.48419805T>A | CA406698441 | GRIN2D | c.2082T>A (p.Ser694Arg) | |
19 | g.48419805T>C | CA508038196 | GRIN2D | c.2082T>C (p.Ser694=) | |
19 | g.48419805T>G | CA406698442 | GRIN2D | c.2082T>G (p.Ser694Arg) | |
19 | g.48419806G>A | CA406698443 | GRIN2D | c.2083G>A (p.Asp695Asn) | |
19 | g.48419806G>C | CA406698445 | GRIN2D | c.2083G>C (p.Asp695His) | |
19 | g.48419806G>T | CA406698444 | GRIN2D | c.2083G>T (p.Asp695Tyr) | gnomAD v4 |
19 | g.48419807A>C | CA406698446 | GRIN2D | c.2084A>C (p.Asp695Ala) | |
19 | g.48419807A>G | CA406698447 | GRIN2D | c.2084A>G (p.Asp695Gly) | gnomAD v4 |
19 | g.48419807A>T | CA406698448 | GRIN2D | c.2084A>T (p.Asp695Val) | |
19 | g.48419808C>A | CA406698449 | GRIN2D | c.2085C>A (p.Asp695Glu) | gnomAD v4 |
19 | g.48419808C>G | CA406698450 | GRIN2D | c.2085C>G (p.Asp695Glu) | |
19 | g.48419808C>T | CA508038197 | GRIN2D | c.2085C>T (p.Asp695=) | |
19 | g.48419809C>A | CA406698451 | GRIN2D | c.2086C>A (p.Arg696Ser) | |
19 | g.48419809C= | CA2339887632 | GRIN2D | c.2086C= (p.Arg696=) | |
19 | g.48419809C>G | CA406698452 | GRIN2D | c.2086C>G (p.Arg696Gly) | |
19 | g.48419809C>T | CA9550638 | GRIN2D | c.2086C>T (p.Arg696Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48419810G>A | CA406698453 | GRIN2D | c.2087G>A (p.Arg696His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.48419810G>C | CA406698454 | GRIN2D | c.2087G>C (p.Arg696Pro) | |
19 | g.48419810G= | CA2339887633 | GRIN2D | c.2087G= (p.Arg696=) | |
19 | g.48419810G>T | CA406698455 | GRIN2D | c.2087G>T (p.Arg696Leu) |