Primary Site >> Stomach Cancer
Gene >> ROR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91737447:91737447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.566G>A |
| AA Mutation | p.Arg189Gln(p.R189Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91731083:91731083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1010G>A |
| AA Mutation | p.Cys337Tyr(p.C337Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91737468:91737468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.545G>A |
| AA Mutation | p.Cys182Tyr(p.C182Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91733316:91733316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743C>T |
| AA Mutation | p.Pro248Leu(p.P248L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724609:91724609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148844963 |
| CDS Mutation | c.1885G>A |
| AA Mutation | p.Val629Met(p.V629M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724749:91724749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368499304 |
| CDS Mutation | c.1745C>T |
| AA Mutation | p.Thr582Met(p.T582M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724167:91724167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2327G>A |
| AA Mutation | p.Ser776Asn(p.S776N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724843:91724843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1651A>G |
| AA Mutation | p.Met551Val(p.M551V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91731098:91731098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.995A>T |
| AA Mutation | p.Lys332Met(p.K332M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91733398:91733398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.661G>T |
| AA Mutation | p.Asp221Tyr(p.D221Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91730992:91730992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1101C>A |
| AA Mutation | p.Asn367Lys(p.N367K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724933:91724933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1561T>G |
| AA Mutation | p.Phe521Val(p.F521V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91733244:91733244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.815G>A |
| AA Mutation | p.Arg272His(p.R272H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724830:91724830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767004305 |
| CDS Mutation | c.1664A>G |
| AA Mutation | p.Tyr555Cys(p.Y555C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724906:91724906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369080860 |
| CDS Mutation | c.1588C>T |
| AA Mutation | p.Arg530Trp(p.R530W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91730915:91730915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754411436 |
| CDS Mutation | c.1178C>T |
| AA Mutation | p.Ser393Leu(p.S393L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375708 |
| Start | 91731078:91731078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1015C>T |
| AA Mutation | p.Pro339Ser(p.P339S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724787:91724787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766805321 |
| CDS Mutation | c.1707G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724664:91724664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138080280 |
| CDS Mutation | c.1830C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724817:91724817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768187491 |
| CDS Mutation | c.1677C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91733396:91733396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.663C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724523:91724523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1971C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724460:91724460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199681534 |
| CDS Mutation | c.2034C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375708 |
| Start | 91724145:91724145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761291207 |
| CDS Mutation | c.2349C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |