Primary Site >> Stomach Cancer
Gene >> GRIN2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564599:13564599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2639G>A |
| AA Mutation | p.Arg880His(p.R880H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564540:13564540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2698C>T |
| AA Mutation | p.Arg900Cys(p.R900C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13562970:13562970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4268C>T |
| AA Mutation | p.Ala1423Val(p.A1423V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563343:13563343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45540034 |
| CDS Mutation | c.3895C>T |
| AA Mutation | p.Arg1299Cys(p.R1299C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564611:13564611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2627C>T |
| AA Mutation | p.Ala876Val(p.A876V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13753324:13753324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003C>A |
| AA Mutation | p.Leu335Ile(p.L335I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13865884:13865884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772078838 |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Ala109Thr(p.A109T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13865872:13865872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337G>A |
| AA Mutation | p.Asp113Asn(p.D113N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563673:13563673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535509676 |
| CDS Mutation | c.3565G>A |
| AA Mutation | p.Val1189Met(p.V1189M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13615162:13615162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1606G>A |
| AA Mutation | p.Val536Ile(p.V536I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563207:13563207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759438353 |
| CDS Mutation | c.4031C>T |
| AA Mutation | p.Ala1344Val(p.A1344V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563922:13563922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199799650 |
| CDS Mutation | c.3316G>A |
| AA Mutation | p.Glu1106Lys(p.E1106K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563202:13563202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766060662 |
| CDS Mutation | c.4036G>A |
| AA Mutation | p.Glu1346Lys(p.E1346K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563613:13563613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3625C>T |
| AA Mutation | p.Arg1209Trp(p.R1209W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564530:13564530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2708G>A |
| AA Mutation | p.Arg903His(p.R903H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13567143:13567143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2480C>A |
| AA Mutation | p.Ala827Glu(p.A827E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13866048:13866048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.161A>G |
| AA Mutation | p.His54Arg(p.H54R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564600:13564600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2638C>T |
| AA Mutation | p.Arg880Cys(p.R880C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13567169:13567169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2454G>T |
| AA Mutation | p.Met818Ile(p.M818I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563441:13563441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201947553 |
| CDS Mutation | c.3797C>T |
| AA Mutation | p.Pro1266Leu(p.P1266L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13615161:13615161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1607T>G |
| AA Mutation | p.Val536Gly(p.V536G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13753872:13753872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.455A>C |
| AA Mutation | p.Gln152Pro(p.Q152P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13615534:13615534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1459G>T |
| AA Mutation | p.Gly487Trp(p.G487W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563211:13563211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4027T>C |
| AA Mutation | p.Ser1343Pro(p.S1343P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564248:13564248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2990C>T |
| AA Mutation | p.Ala997Val(p.A997V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563317:13563317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3921C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563689:13563689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201568782 |
| CDS Mutation | c.3549G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13865873:13865873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13615514:13615514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1479C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13753670:13753670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.657G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13562981:13562981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761174489 |
| CDS Mutation | c.4257G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13562966:13562966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4272T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563899:13563899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200660626 |
| CDS Mutation | c.3339G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13562837:13562837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4401C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563281:13563281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141730031 |
| CDS Mutation | c.3957G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563593:13563593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3645C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563674:13563674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13564484:13564484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756487785 |
| CDS Mutation | c.2754G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000609686 |
| Start | 13563487:13563487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200186058 |
| CDS Mutation | c.3751C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |