Primary Site >> Stomach Cancer
Gene >> GALNT18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11379189:11379189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748397179 |
| CDS Mutation | c.671G>A |
| AA Mutation | p.Arg224His(p.R224H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11332813:11332813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1297G>T |
| AA Mutation | p.Gly433Trp(p.G433W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000227756 |
| Start | 11379263:11379263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.597G>T |
| AA Mutation | p.Glu199Asp(p.E199D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11448787:11448787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377131654 |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Cys(p.R129C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11377372:11377372(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787C>G |
| AA Mutation | p.Pro263Ala(p.P263A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11372536:11372536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1071G>T |
| AA Mutation | p.Glu357Asp(p.E357D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11621485:11621485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Ala37Thr(p.A37T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11448801:11448801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.371C>T |
| AA Mutation | p.Ala124Val(p.A124V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11293190:11293190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779824658 |
| CDS Mutation | c.1516G>A |
| AA Mutation | p.Val506Met(p.V506M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11432758:11432758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.458T>C |
| AA Mutation | p.Leu153Pro(p.L153P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000227756 |
| Start | 11432621:11432621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746409394 |
| CDS Mutation | c.595G>A |
| AA Mutation | p.Glu199Lys(p.E199K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11377366:11377366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.793C>T |
| AA Mutation | p.Leu265Phe(p.L265F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11621457:11621457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.137C>T |
| AA Mutation | p.Pro46Leu(p.P46L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227756 |
| Start | 11271196:11271196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1772G>A |
| AA Mutation | p.Cys591Tyr(p.C591Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227756 |
| Start | 11340912:11340912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577502852 |
| CDS Mutation | c.1185C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227756 |
| Start | 11448812:11448812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151161334 |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227756 |
| Start | 11372602:11372602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1005T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227756 |
| Start | 11332715:11332715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368510206 |
| CDS Mutation | c.1395C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000227756 |
| Start | 11379146:11379169(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.691_714delCTCATCCGCTCCAGGGTCAGTGGC |
| AA Mutation | p.Leu231_Gly238del(p.L231_G238del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |