Primary Site >> Stomach Cancer
Gene >> RHOBTB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23017381:23017381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763030083 |
| CDS Mutation | c.2096G>A |
| AA Mutation | p.Arg699Gln(p.R699Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007384:23007384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778573219 |
| CDS Mutation | c.1139C>T |
| AA Mutation | p.Pro380Leu(p.P380L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23017329:23017329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371598054 |
| CDS Mutation | c.2044C>T |
| AA Mutation | p.Arg682Trp(p.R682W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23008085:23008085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1594C>G |
| AA Mutation | p.Pro532Ala(p.P532A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007368:23007368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759105470 |
| CDS Mutation | c.1123G>A |
| AA Mutation | p.Gly375Arg(p.G375R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23010557:23010557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202072436 |
| CDS Mutation | c.1640G>A |
| AA Mutation | p.Ser547Asn(p.S547N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23005968:23005968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.305T>C |
| AA Mutation | p.Val102Ala(p.V102A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23006913:23006913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375369739 |
| CDS Mutation | c.668A>G |
| AA Mutation | p.Asn223Ser(p.N223S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23010656:23010656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757818105 |
| CDS Mutation | c.1739G>A |
| AA Mutation | p.Arg580His(p.R580H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007698:23007698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1453C>T |
| AA Mutation | p.Arg485Cys(p.R485C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23017330:23017330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143264894 |
| CDS Mutation | c.2045G>A |
| AA Mutation | p.Arg682Gln(p.R682Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23010655:23010655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1738C>T |
| AA Mutation | p.Arg580Cys(p.R580C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007332:23007332(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757015873 |
| CDS Mutation | c.1087C>T |
| AA Mutation | p.Arg363Cys(p.R363C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007572:23007572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1327C>T |
| AA Mutation | p.Arg443Cys(p.R443C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23005988:23005988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325A>G |
| AA Mutation | p.Ile109Val(p.I109V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23017383:23017383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370025125 |
| CDS Mutation | c.2098C>T |
| AA Mutation | p.Arg700Cys(p.R700C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000251822 |
| Start | 23005388:23005388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775527995 |
| CDS Mutation | c.209G>A |
| AA Mutation | p.Arg70Gln(p.R70Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251822 |
| Start | 23004620:23004620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007349:23007349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747030867 |
| CDS Mutation | c.1104C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251822 |
| Start | 23006968:23006968(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765307995 |
| CDS Mutation | c.723G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000251822 |
| Start | 23006734:23006734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.489C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251822 |
| Start | 23008079:23008079(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1593delG |
| AA Mutation | p.Pro532HisfsTer41(p.P532Hfs*41) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000251822 |
| Start | 23007159:23007160(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.920dupG |
| AA Mutation | p.Ser309LeufsTer16(p.S309Lfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |