Primary Site >> Stomach Cancer
Gene >> GAL3ST1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555320:30555320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905T>C |
| AA Mutation | p.Met302Thr(p.M302T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30556004:30556004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221C>T |
| AA Mutation | p.Pro74Leu(p.P74L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555207:30555207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018C>T |
| AA Mutation | p.Arg340Cys(p.R340C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555381:30555381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769892145 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Cys(p.R282C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555423:30555423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.802T>C |
| AA Mutation | p.Trp268Arg(p.W268R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555255:30555255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.970C>T |
| AA Mutation | p.Arg324Trp(p.R324W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338911 |
| Start | 30556007:30556007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.218A>G |
| AA Mutation | p.Gln73Arg(p.Q73R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555868:30555868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.357C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555175:30555175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555429:30555429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.796C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555889:30555889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000338911 |
| Start | 30556075:30556075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs73394272 |
| CDS Mutation | c.150G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555351:30555351(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.874delG |
| AA Mutation | p.Glu292SerfsTer110(p.E292Sfs*110) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555328:30555328(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.897delC |
| AA Mutation | p.Trp300GlyfsTer102(p.W300Gfs*102) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000338911 |
| Start | 30555178:30555179(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1046dupG |
| AA Mutation | p.His350ProfsTer93(p.H350Pfs*93) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |