Primary Site >> Stomach Cancer
Gene >> SUSD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24187298:24187298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1739T>G |
| AA Mutation | p.Val580Gly(p.V580G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24184210:24184210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776858506 |
| CDS Mutation | c.514G>A |
| AA Mutation | p.Ala172Thr(p.A172T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24185873:24185873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1283G>T |
| AA Mutation | p.Arg428Leu(p.R428L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24184810:24184810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652T>C |
| AA Mutation | p.Tyr218His(p.Y218H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000358321 |
| Start | 24188327:24188327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2444C>T |
| AA Mutation | p.Thr815Met(p.T815M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24184190:24184190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139840706 |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Arg165His(p.R165H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24187348:24187348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765493836 |
| CDS Mutation | c.1789G>A |
| AA Mutation | p.Gly597Arg(p.G597R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24185755:24185755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375763524 |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Gly389Ser(p.G389S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358321 |
| Start | 24187603:24187603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1924T>C |
| AA Mutation | p.Tyr642His(p.Y642H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24188235:24188235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779537380 |
| CDS Mutation | c.2352C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24185787:24185787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757766939 |
| CDS Mutation | c.1197G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24186149:24186149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1473G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24183202:24183202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.222C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24184182:24184182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201161910 |
| CDS Mutation | c.486C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358321 |
| Start | 24185700:24185700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765294488 |
| CDS Mutation | c.1110G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |