| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.113412755A= | CA2001168001 | DRD2 | c.939T= (p.His313=) c.852T= (p.His284=) c.945T= (p.His315=) c.936T= (p.His312=) | |
| 11 | g.113412755A>C | CA382650257 | DRD2 | c.939T>G (p.His313Gln) c.852T>G (p.His284Gln) c.945T>G (p.His315Gln) c.936T>G (p.His312Gln) | |
| 11 | g.113412755A>G | CA6281224 | DRD2 | c.939T>C (p.His313=) c.852T>C (p.His284=) c.945T>C (p.His315=) c.936T>C (p.His312=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.113412755A>T | CA382650255 | DRD2 | c.939T>A (p.His313Gln) c.852T>A (p.His284Gln) c.945T>A (p.His315Gln) c.936T>A (p.His312Gln) | gnomAD v3 gnomAD v4 |
| 11 | g.113412756T>A | CA382650258 | DRD2 | c.938A>T (p.His313Leu) c.851A>T (p.His284Leu) c.944A>T (p.His315Leu) c.935A>T (p.His312Leu) | |
| 11 | g.113412756T>C | CA228625670 | DRD2 | c.938A>G (p.His313Arg) c.851A>G (p.His284Arg) c.944A>G (p.His315Arg) c.935A>G (p.His312Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.113412756T>G | CA382650261 | DRD2 | c.938A>C (p.His313Pro) c.851A>C (p.His284Pro) c.944A>C (p.His315Pro) c.935A>C (p.His312Pro) | |
| 11 | g.113412756T= | CA2001168002 | DRD2 | c.938A= (p.His313=) c.851A= (p.His284=) c.944A= (p.His315=) c.935A= (p.His312=) | |
| 11 | g.113412757G>A | CA382650263 | DRD2 | c.937C>T (p.His313Tyr) c.850C>T (p.His284Tyr) c.943C>T (p.His315Tyr) c.934C>T (p.His312Tyr) | |
| 11 | g.113412757G>C | CA382650265 | DRD2 | c.937C>G (p.His313Asp) c.850C>G (p.His284Asp) c.943C>G (p.His315Asp) c.934C>G (p.His312Asp) | |
| 11 | g.113412757G>T | CA382650267 | DRD2 | c.937C>A (p.His313Asn) c.850C>A (p.His284Asn) c.943C>A (p.His315Asn) c.934C>A (p.His312Asn) | |
| 11 | g.113412758G>A | CA6281225 | DRD2 | c.936C>T (p.His312=) c.849C>T (p.His283=) c.942C>T (p.His314=) c.933C>T (p.His311=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.113412758G>C | CA382650270 | DRD2 | c.936C>G (p.His312Gln) c.849C>G (p.His283Gln) c.942C>G (p.His314Gln) c.933C>G (p.His311Gln) | |
| 11 | g.113412758G= | CA2001168003 | DRD2 | c.936C= (p.His312=) c.849C= (p.His283=) c.942C= (p.His314=) c.933C= (p.His311=) | |
| 11 | g.113412758G>T | CA382650272 | DRD2 | c.936C>A (p.His312Gln) c.849C>A (p.His283Gln) c.942C>A (p.His314Gln) c.933C>A (p.His311Gln) | |
| 11 | g.113412759T>A | CA382650276 | DRD2 | c.935A>T (p.His312Leu) c.848A>T (p.His283Leu) c.941A>T (p.His314Leu) c.932A>T (p.His311Leu) | |
| 11 | g.113412759T>C | CA382650275 | DRD2 | c.935A>G (p.His312Arg) c.848A>G (p.His283Arg) c.941A>G (p.His314Arg) c.932A>G (p.His311Arg) | |
| 11 | g.113412759T>G | CA382650274 | DRD2 | c.935A>C (p.His312Pro) c.848A>C (p.His283Pro) c.941A>C (p.His314Pro) c.932A>C (p.His311Pro) | |
| 11 | g.113412760G>A | CA382650277 | DRD2 | c.934C>T (p.His312Tyr) c.847C>T (p.His283Tyr) c.940C>T (p.His314Tyr) c.931C>T (p.His311Tyr) | dbSNP gnomAD v4 |
| 11 | g.113412760G>C | CA382650279 | DRD2 | c.934C>G (p.His312Asp) c.847C>G (p.His283Asp) c.940C>G (p.His314Asp) c.931C>G (p.His311Asp) | |
| 11 | g.113412760G= | CA2001168004 | DRD2 | c.934C= (p.His312=) c.847C= (p.His283=) c.940C= (p.His314=) c.931C= (p.His311=) | |
| 11 | g.113412760G>T | CA382650281 | DRD2 | c.934C>A (p.His312Asn) c.847C>A (p.His283Asn) c.940C>A (p.His314Asn) c.931C>A (p.His311Asn) | |
| 11 | g.113412761G>A | CA477043209 | DRD2 | c.933C>T (p.Ser311=) c.846C>T (p.Ser282=) c.939C>T (p.Ser313=) c.930C>T (p.Ser310=) | gnomAD v4 |
| 11 | g.113412761G>C | CA477043210 | DRD2 | c.933C>G (p.Ser311=) c.846C>G (p.Ser282=) c.939C>G (p.Ser313=) c.930C>G (p.Ser310=) | |
| 11 | g.113412761G>T | CA477043211 | DRD2 | c.933C>A (p.Ser311=) c.846C>A (p.Ser282=) c.939C>A (p.Ser313=) c.930C>A (p.Ser310=) | |
| 11 | g.113412762G>A | CA382650282 | DRD2 | c.932C>T (p.Ser311Phe) c.845C>T (p.Ser282Phe) c.938C>T (p.Ser313Phe) c.929C>T (p.Ser310Phe) | |
| 11 | g.113412762G>C | CA6281226 | DRD2 | c.932C>G (p.Ser311Cys) c.845C>G (p.Ser282Cys) c.938C>G (p.Ser313Cys) c.929C>G (p.Ser310Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.113412762G= | CA2001168005 | DRD2 | c.932C= (p.Ser311=) c.845C= (p.Ser282=) c.938C= (p.Ser313=) c.929C= (p.Ser310=) | |
| 11 | g.113412762G>T | CA382650284 | DRD2 | c.932C>A (p.Ser311Tyr) c.845C>A (p.Ser282Tyr) c.938C>A (p.Ser313Tyr) c.929C>A (p.Ser310Tyr) | |
| 11 | g.113412763A= | CA2001168006 | DRD2 | c.931T= (p.Ser311=) c.844T= (p.Ser282=) c.937T= (p.Ser313=) c.928T= (p.Ser310=) | |
| 11 | g.113412763A>C | CA382650286 | DRD2 | c.931T>G (p.Ser311Ala) c.844T>G (p.Ser282Ala) c.937T>G (p.Ser313Ala) c.928T>G (p.Ser310Ala) | |
| 11 | g.113412763A>G | CA382650288 | DRD2 | c.931T>C (p.Ser311Pro) c.844T>C (p.Ser282Pro) c.937T>C (p.Ser313Pro) c.928T>C (p.Ser310Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.113412763A>T | CA382650290 | DRD2 | c.931T>A (p.Ser311Thr) c.844T>A (p.Ser282Thr) c.937T>A (p.Ser313Thr) c.928T>A (p.Ser310Thr) | |
| 11 | g.113412764C>A | CA477043212 | DRD2 | c.930G>T (p.Pro310=) c.843G>T (p.Pro281=) c.936G>T (p.Pro312=) c.927G>T (p.Pro309=) | |
| 11 | g.113412764C= | CA2001168007 | DRD2 | c.930G= (p.Pro310=) c.843G= (p.Pro281=) c.936G= (p.Pro312=) c.927G= (p.Pro309=) | |
| 11 | g.113412764C>G | CA477043213 | DRD2 | c.930G>C (p.Pro310=) c.843G>C (p.Pro281=) c.936G>C (p.Pro312=) c.927G>C (p.Pro309=) | |
| 11 | g.113412764C>T | CA6281227 | DRD2 | c.930G>A (p.Pro310=) c.843G>A (p.Pro281=) c.936G>A (p.Pro312=) c.927G>A (p.Pro309=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 11 | g.113412765G>A | CA6281228 | DRD2 | c.929C>T (p.Pro310Leu) c.842C>T (p.Pro281Leu) c.935C>T (p.Pro312Leu) c.926C>T (p.Pro309Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.113412765G>C | CA382650293 | DRD2 | c.929C>G (p.Pro310Arg) c.842C>G (p.Pro281Arg) c.935C>G (p.Pro312Arg) c.926C>G (p.Pro309Arg) | |
| 11 | g.113412765G= | CA2001168008 | DRD2 | c.929C= (p.Pro310=) c.842C= (p.Pro281=) c.935C= (p.Pro312=) c.926C= (p.Pro309=) | |
| 11 | g.113412765G>T | CA382650295 | DRD2 | c.929C>A (p.Pro310Gln) c.842C>A (p.Pro281Gln) c.935C>A (p.Pro312Gln) c.926C>A (p.Pro309Gln) | |
| 11 | g.113412766G>A | CA6281229 | DRD2 | c.928C>T (p.Pro310Ser) c.841C>T (p.Pro281Ser) c.934C>T (p.Pro312Ser) c.925C>T (p.Pro309Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.113412766G>C | CA382650299 | DRD2 | c.928C>G (p.Pro310Ala) c.841C>G (p.Pro281Ala) c.934C>G (p.Pro312Ala) c.925C>G (p.Pro309Ala) | |
| 11 | g.113412766G= | CA2001168009 | DRD2 | c.928C= (p.Pro310=) c.841C= (p.Pro281=) c.934C= (p.Pro312=) c.925C= (p.Pro309=) | |
| 11 | g.113412766G>T | CA382650297 | DRD2 | c.928C>A (p.Pro310Thr) c.841C>A (p.Pro281Thr) c.934C>A (p.Pro312Thr) c.925C>A (p.Pro309Thr) | |
| 11 | g.113412767G>A | CA477043216 | DRD2 | c.927C>T (p.Asp309=) c.840C>T (p.Asp280=) c.933C>T (p.Asp311=) c.924C>T (p.Asp308=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.113412767G>C | CA382650301 | DRD2 | c.927C>G (p.Asp309Glu) c.840C>G (p.Asp280Glu) c.933C>G (p.Asp311Glu) c.924C>G (p.Asp308Glu) | |
| 11 | g.113412767G= | CA2001168010 | DRD2 | c.927C= (p.Asp309=) c.840C= (p.Asp280=) c.933C= (p.Asp311=) c.924C= (p.Asp308=) | |
| 11 | g.113412767G>T | CA382650303 | DRD2 | c.927C>A (p.Asp309Glu) c.840C>A (p.Asp280Glu) c.933C>A (p.Asp311Glu) c.924C>A (p.Asp308Glu) | |
| 11 | g.113412768T>A | CA382650305 | DRD2 | c.926A>T (p.Asp309Val) c.839A>T (p.Asp280Val) c.932A>T (p.Asp311Val) c.923A>T (p.Asp308Val) |