Primary Site >> Stomach Cancer
Gene >> SUCO
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172588968:172588968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1867A>C |
| AA Mutation | p.Ile623Leu(p.I623L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172589034:172589034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754869865 |
| CDS Mutation | c.1933C>T |
| AA Mutation | p.Arg645Trp(p.R645W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172570058:172570058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868C>T |
| AA Mutation | p.His290Tyr(p.H290Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172609885:172609885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3391G>A |
| AA Mutation | p.Ala1131Thr(p.A1131T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172600131:172600131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2981C>T |
| AA Mutation | p.Ser994Leu(p.S994L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172551591:172551591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142G>A |
| AA Mutation | p.Ala48Thr(p.A48T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172589764:172589764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2663A>G |
| AA Mutation | p.Tyr888Cys(p.Y888C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172589670:172589670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2569G>A |
| AA Mutation | p.Val857Met(p.V857M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172585036:172585036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1517T>C |
| AA Mutation | p.Val506Ala(p.V506A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172569076:172569076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.790G>T |
| AA Mutation | p.Asp264Tyr(p.D264Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263688 |
| Start | 172589019:172589019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1918A>G |
| AA Mutation | p.Arg640Gly(p.R640G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263688 |
| Start | 172610178:172610178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767035513 |
| CDS Mutation | c.3684G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |