Primary Site >> Stomach Cancer
Gene >> MYBL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43716067:43716067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2083C>T |
| AA Mutation | p.Arg695Trp(p.R695W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43699955:43699955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.862C>A |
| AA Mutation | p.Leu288Met(p.L288M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43699880:43699880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775568667 |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Ala263Thr(p.A263T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43715230:43715230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139167760 |
| CDS Mutation | c.1921G>A |
| AA Mutation | p.Glu641Lys(p.E641K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43673853:43673853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750982841 |
| CDS Mutation | c.68C>T |
| AA Mutation | p.Pro23Leu(p.P23L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43682856:43682856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.249G>T |
| AA Mutation | p.Lys83Asn(p.K83N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43686943:43686943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.371G>A |
| AA Mutation | p.Arg124His(p.R124H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43682798:43682798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149840592 |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Arg64His(p.R64H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000217026 |
| Start | 43710030:43710030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Ala525Thr(p.A525T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43699813:43699813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.720C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43702894:43702894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1356G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43716072:43716072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200062988 |
| CDS Mutation | c.2088C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43686989:43686989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146572896 |
| CDS Mutation | c.417C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43710011:43710011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1554G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43702750:43702750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1212C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43699783:43699783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745706704 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43715197:43715197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1888T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43681822:43681822(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.153G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43686938:43686938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.366T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000217026 |
| Start | 43692286:43692286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746709523 |
| CDS Mutation | c.630C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |