Primary Site >> Stomach Cancer
Gene >> ARSI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297437:150297437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1487A>G |
| AA Mutation | p.Asn496Ser(p.N496S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150298245:150298245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775003019 |
| CDS Mutation | c.679C>T |
| AA Mutation | p.Arg227Cys(p.R227C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297800:150297800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374583135 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Pro375Leu(p.P375L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150298103:150298103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.821T>G |
| AA Mutation | p.Val274Gly(p.V274G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297497:150297497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1427A>G |
| AA Mutation | p.Asp476Gly(p.D476G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297387:150297387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1537C>T |
| AA Mutation | p.Pro513Ser(p.P513S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297909:150297909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149628658 |
| CDS Mutation | c.1015C>T |
| AA Mutation | p.Arg339Trp(p.R339W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297926:150297926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998T>C |
| AA Mutation | p.Leu333Pro(p.L333P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328668 |
| Start | 150298267:150298267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.657C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297586:150297586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570157787 |
| CDS Mutation | c.1338G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297766:150297766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757161790 |
| CDS Mutation | c.1158G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000328668 |
| Start | 150297253:150297254(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1670dupT |
| AA Mutation | p.Arg558ProfsTer2(p.R558Pfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |