Primary Site >> Stomach Cancer
Gene >> GRID1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206441:86206441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150264113 |
| CDS Mutation | c.443G>A |
| AA Mutation | p.Arg148His(p.R148H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85647347:85647347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76097378 |
| CDS Mutation | c.2048G>A |
| AA Mutation | p.Arg683Gln(p.R683Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85619904:85619904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2323C>A |
| AA Mutation | p.Gln775Lys(p.Q775K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85602650:85602650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2653G>A |
| AA Mutation | p.Asp885Asn(p.D885N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206531:86206531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751158483 |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Arg118His(p.R118H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724452:85724452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1758A>G |
| AA Mutation | p.Ile586Met(p.I586M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206511:86206511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.373C>T |
| AA Mutation | p.Arg125Cys(p.R125C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85613592:85613592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775121477 |
| CDS Mutation | c.2416C>T |
| AA Mutation | p.Pro806Ser(p.P806S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86138911:86138911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.634A>T |
| AA Mutation | p.Met212Leu(p.M212L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85856060:85856060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1082G>A |
| AA Mutation | p.Gly361Asp(p.G361D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85647315:85647315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2080A>G |
| AA Mutation | p.Lys694Glu(p.K694E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206478:86206478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777504912 |
| CDS Mutation | c.406G>A |
| AA Mutation | p.Gly136Ser(p.G136S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85727955:85727955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433T>C |
| AA Mutation | p.Leu478Pro(p.L478P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85723103:85723103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770160415 |
| CDS Mutation | c.1897G>A |
| AA Mutation | p.Val633Met(p.V633M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85856151:85856151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.991G>A |
| AA Mutation | p.Ala331Thr(p.A331T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724565:85724565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371004026 |
| CDS Mutation | c.1645G>A |
| AA Mutation | p.Glu549Lys(p.E549K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86364093:86364093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.83C>T |
| AA Mutation | p.Ala28Val(p.A28V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85613528:85613528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2480A>T |
| AA Mutation | p.Lys827Met(p.K827M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724570:85724570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1640A>C |
| AA Mutation | p.Lys547Thr(p.K547T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85723136:85723136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148165863 |
| CDS Mutation | c.1864G>A |
| AA Mutation | p.Glu622Lys(p.E622K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724445:85724445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1765G>A |
| AA Mutation | p.Val589Met(p.V589M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206510:86206510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.374G>A |
| AA Mutation | p.Arg125His(p.R125H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 86138848:86138848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.697C>A |
| AA Mutation | p.Pro233Thr(p.P233T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85729532:85729532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751523472 |
| CDS Mutation | c.1316T>C |
| AA Mutation | p.Leu439Pro(p.L439P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85602529:85602529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2774T>G |
| AA Mutation | p.Leu925Arg(p.L925R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724520:85724520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1690G>T |
| AA Mutation | p.Ala564Ser(p.A564S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85602429:85602429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2874G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724566:85724566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577558971 |
| CDS Mutation | c.1644C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206446:86206446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764843634 |
| CDS Mutation | c.438C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85602318:85602318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754049968 |
| CDS Mutation | c.2985C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85723053:85723053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1947A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85647232:85647232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374077562 |
| CDS Mutation | c.2163C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85727882:85727882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201170791 |
| CDS Mutation | c.1506C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 86206470:86206470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.414C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85724521:85724521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs558668541 |
| CDS Mutation | c.1689C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000327946 |
| Start | 85856146:85856146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368514571 |
| CDS Mutation | c.996C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |