Primary Site >> Stomach Cancer
Gene >> MST1R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49896272:49896272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751338048 |
| CDS Mutation | c.2572C>T |
| AA Mutation | p.Arg858Cys(p.R858C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49890590:49890590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3705C>G |
| AA Mutation | p.Asp1235Glu(p.D1235E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49902589:49902589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760389915 |
| CDS Mutation | c.1021G>A |
| AA Mutation | p.Glu341Lys(p.E341K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898634:49898634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1603C>T |
| AA Mutation | p.Arg535Cys(p.R535C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898923:49898923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148258933 |
| CDS Mutation | c.1492G>A |
| AA Mutation | p.Val498Met(p.V498M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898657:49898657(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1580G>A |
| AA Mutation | p.Cys527Tyr(p.C527Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49903048:49903048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562G>A |
| AA Mutation | p.Val188Met(p.V188M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898875:49898875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1540G>C |
| AA Mutation | p.Gly514Arg(p.G514R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49903011:49903011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.599C>G |
| AA Mutation | p.Ala200Gly(p.A200G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898160:49898160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1771G>T |
| AA Mutation | p.Gly591Cys(p.G591C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000296474 |
| Start | 49897281:49897281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201008581 |
| CDS Mutation | c.2182C>T |
| AA Mutation | p.Arg728Trp(p.R728W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49902423:49902423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781591594 |
| CDS Mutation | c.1187G>A |
| AA Mutation | p.Arg396Gln(p.R396Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898916:49898916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755080567 |
| CDS Mutation | c.1499G>A |
| AA Mutation | p.Arg500Gln(p.R500Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898543:49898543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1694A>T |
| AA Mutation | p.Asp565Val(p.D565V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296474 |
| Start | 49898888:49898888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1527A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296474 |
| Start | 49890569:49890569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3726A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296474 |
| Start | 49903511:49903511(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.99delC |
| AA Mutation | p.Tyr34ThrfsTer9(p.Y34Tfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000296474 |
| Start | 49903528:49903528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774953632 |
| CDS Mutation | c.82C>T |
| AA Mutation | p.Gln28Ter(p.Q28*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000296474 |
| Start | 49902678:49902679(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs760002850 |
| CDS Mutation | c.931dupG |
| AA Mutation | p.Ala311GlyfsTer26(p.A311Gfs*26) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |