Primary Site >> Stomach Cancer
Gene >> GRIK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 102035394:102035394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2139G>T |
| AA Mutation | p.Arg713Ser(p.R713S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626539:101626539(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443G>A |
| AA Mutation | p.Ser148Asn(p.S148N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101928594:101928594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2047G>A |
| AA Mutation | p.Gly683Arg(p.G683R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101799658:101799658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962C>T |
| AA Mutation | p.Ala321Val(p.A321V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626395:101626395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.299C>A |
| AA Mutation | p.Ser100Tyr(p.S100Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101686324:101686324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767667188 |
| CDS Mutation | c.922G>A |
| AA Mutation | p.Asp308Asn(p.D308N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101676698:101676698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.617C>A |
| AA Mutation | p.Ala206Asp(p.A206D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101924638:101924638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1786A>C |
| AA Mutation | p.Asn596His(p.N596H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101818455:101818455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1289A>G |
| AA Mutation | p.Asn430Ser(p.N430S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101676712:101676712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631G>T |
| AA Mutation | p.Ala211Ser(p.A211S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101859437:101859437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1468G>T |
| AA Mutation | p.Ala490Ser(p.A490S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101621982:101621982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149T>G |
| AA Mutation | p.Met50Arg(p.M50R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101622086:101622086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143873289 |
| CDS Mutation | c.253C>A |
| AA Mutation | p.Leu85Ile(p.L85I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101818458:101818458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1292G>A |
| AA Mutation | p.Arg431His(p.R431H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101399291:101399291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14T>A |
| AA Mutation | p.Phe5Tyr(p.F5Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626485:101626485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.389T>C |
| AA Mutation | p.Ile130Thr(p.I130T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 102035523:102035523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758586743 |
| CDS Mutation | c.2268C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 102035358:102035358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556175755 |
| CDS Mutation | c.2103G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 101859388:101859388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1419C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626438:101626438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.342A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626615:101626615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147153195 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 101799761:101799761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542238643 |
| CDS Mutation | c.1065C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000421544 |
| Start | 101626621:101626621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.525G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000421544 |
| Start | 102055557:102055557(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs766825430 |
| CDS Mutation | c.2546delA |
| AA Mutation | p.Asn849ThrfsTer14(p.N849Tfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |