Primary Site >> Stomach Cancer
Gene >> BAG3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119670056:119670056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386C>T |
| AA Mutation | p.Ala129Val(p.A129V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119676909:119676909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1355T>C |
| AA Mutation | p.Leu452Pro(p.L452P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119651719:119651719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.44G>A |
| AA Mutation | p.Gly15Asp(p.G15D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369085 |
| Start | 119672255:119672255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200479768 |
| CDS Mutation | c.508C>T |
| AA Mutation | p.Arg170Trp(p.R170W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119676967:119676967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1413G>T |
| AA Mutation | p.Glu471Asp(p.E471D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119676936:119676936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382A>T |
| AA Mutation | p.Glu461Val(p.E461V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369085 |
| Start | 119676873:119676873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1319A>G |
| AA Mutation | p.Asp440Gly(p.D440G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369085 |
| Start | 119676610:119676610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1056C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369085 |
| Start | 119669901:119669901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143752613 |
| CDS Mutation | c.231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369085 |
| Start | 119669976:119669976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202006167 |
| CDS Mutation | c.306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369085 |
| Start | 119651742:119651742(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.72delC |
| AA Mutation | p.Gly25AspfsTer186(p.G25Dfs*186) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369085 |
| Start | 119676587:119676587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1033G>T |
| AA Mutation | p.Glu345Ter(p.E345*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369085 |
| Start | 119651741:119651742(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772351208 |
| CDS Mutation | c.72dupC |
| AA Mutation | p.Gly25ArgfsTer33(p.G25Rfs*33) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000369085 |
| Start | 119672283:119672284(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.546_551dupATCCTC |
| AA Mutation | p.Ser184_Ser185dup(p.S184_S185dup) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |