Primary Site >> Stomach Cancer
Gene >> MYO5B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49962285:49962285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1526T>G |
| AA Mutation | p.Leu509Arg(p.L509R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49906620:49906620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2213A>G |
| AA Mutation | p.Lys738Arg(p.K738R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49837583:49837583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5072C>T |
| AA Mutation | p.Ala1691Val(p.A1691V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49856847:49856847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557902503 |
| CDS Mutation | c.3988G>A |
| AA Mutation | p.Gly1330Ser(p.G1330S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49937352:49937352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Pro600Ser(p.P600S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000285039 |
| Start | 49962268:49962268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1543A>G |
| AA Mutation | p.Lys515Glu(p.K515E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 50040179:50040179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372682296 |
| CDS Mutation | c.274C>T |
| AA Mutation | p.Arg92Cys(p.R92C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000285039 |
| Start | 49974471:49974471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761492029 |
| CDS Mutation | c.1201C>T |
| AA Mutation | p.Arg401Cys(p.R401C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49984764:49984764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768088806 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49904798:49904798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372848572 |
| CDS Mutation | c.2445G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49836756:49836756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs1058514 |
| CDS Mutation | c.5268C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49843316:49843316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368186579 |
| CDS Mutation | c.4536G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49875774:49875774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3450G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000285039 |
| Start | 49875725:49875725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3499C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000285039 |
| Start | 49864161:49864161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760030699 |
| CDS Mutation | c.3823C>T |
| AA Mutation | p.Arg1275Ter(p.R1275*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000285039 |
| Start | 49954429:49954430(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1551dupC |
| AA Mutation | p.Lys518GlnfsTer4(p.K518Qfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |