Primary Site >> Stomach Cancer
Gene >> STS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7349912:7349912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1403T>C |
| AA Mutation | p.Phe468Ser(p.F468S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7259637:7259637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.686T>C |
| AA Mutation | p.Leu229Pro(p.L229P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7259403:7259403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452C>A |
| AA Mutation | p.Pro151His(p.P151H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7253264:7253264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.80C>T |
| AA Mutation | p.Pro27Leu(p.P27L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7334035:7334035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766488360 |
| CDS Mutation | c.1306C>T |
| AA Mutation | p.Arg436Cys(p.R436C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7334036:7334036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146965552 |
| CDS Mutation | c.1307G>A |
| AA Mutation | p.Arg436His(p.R436H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7350002:7350002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1493A>G |
| AA Mutation | p.Asp498Gly(p.D498G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7257322:7257322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Ser78Asn(p.S78N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7259468:7259468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.517G>A |
| AA Mutation | p.Gly173Arg(p.G173R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7350208:7350208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1699G>A |
| AA Mutation | p.Gly567Ser(p.G567S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217961 |
| Start | 7259403:7259403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452C>T |
| AA Mutation | p.Pro151Leu(p.P151L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217961 |
| Start | 7350066:7350066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749953304 |
| CDS Mutation | c.1557C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000217961 |
| Start | 7257497:7257528(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.308_339delTCTTCACAGCCTCTTCGGGAGGACTTCCCACC |
| AA Mutation | p.Leu103ArgfsTer2(p.L103Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |