Primary Site >> Stomach Cancer
Gene >> SKI
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378536 |
| Start | 2306185:2306185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1933C>T |
| AA Mutation | p.Arg645Trp(p.R645W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378536 |
| Start | 2303307:2303307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768924434 |
| CDS Mutation | c.1118G>A |
| AA Mutation | p.Arg373His(p.R373H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378536 |
| Start | 2303313:2303313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762209697 |
| CDS Mutation | c.1124G>A |
| AA Mutation | p.Arg375His(p.R375H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000378536 |
| Start | 2229734:2229734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.968G>A |
| AA Mutation | p.Arg323Gln(p.R323Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378536 |
| Start | 2303041:2303041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150934009 |
| CDS Mutation | c.1033G>A |
| AA Mutation | p.Ala345Thr(p.A345T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378536 |
| Start | 2304033:2304033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1405G>A |
| AA Mutation | p.Ala469Thr(p.A469T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378536 |
| Start | 2303891:2303891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773045410 |
| CDS Mutation | c.1263C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378536 |
| Start | 2304038:2304038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150985728 |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378536 |
| Start | 2306184:2306184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1932G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378536 |
| Start | 2229039:2229039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |