Primary Site >> Stomach Cancer
Gene >> VPS53
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571805 |
| Start | 631588:631588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.649G>T |
| AA Mutation | p.Ala217Ser(p.A217S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571805 |
| Start | 627270:627270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749809497 |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Arg293His(p.R293H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571805 |
| Start | 631572:631572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138639431 |
| CDS Mutation | c.665C>T |
| AA Mutation | p.Ala222Val(p.A222V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000571805 |
| Start | 623652:623652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145041715 |
| CDS Mutation | c.997C>T |
| AA Mutation | p.Arg333Cys(p.R333C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571805 |
| Start | 562646:562646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775132136 |
| CDS Mutation | c.1413C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571805 |
| Start | 631571:631571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000571805 |
| Start | 655915:655915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765870836 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000571805 |
| Start | 710586:710586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775421682 |
| CDS Mutation | c.115C>T |
| AA Mutation | p.Arg39Ter(p.R39*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000571805 |
| Start | 627186:627187(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.961dupT |
| AA Mutation | p.Cys321LeufsTer20(p.C321Lfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |