Primary Site >> Stomach Cancer
Gene >> DAB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39376781:39376781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201522659 |
| CDS Mutation | c.2006G>A |
| AA Mutation | p.Arg669Gln(p.R669Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000320816 |
| Start | 39388800:39388800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772234206 |
| CDS Mutation | c.623C>T |
| AA Mutation | p.Ser208Leu(p.S208L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39383256:39383256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.703C>A |
| AA Mutation | p.Leu235Met(p.L235M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39376882:39376882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1905T>G |
| AA Mutation | p.Asp635Glu(p.D635E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39390463:39390463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.443C>T |
| AA Mutation | p.Ala148Val(p.A148V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39388824:39388824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.599A>C |
| AA Mutation | p.Asp200Ala(p.D200A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39381597:39381597(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1361T>G |
| AA Mutation | p.Leu454Arg(p.L454R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39393373:39393373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.112T>C |
| AA Mutation | p.Tyr38His(p.Y38H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39377031:39377031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1756A>G |
| AA Mutation | p.Thr586Ala(p.T586A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39377039:39377039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761659376 |
| CDS Mutation | c.1748C>T |
| AA Mutation | p.Ala583Val(p.A583V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39376955:39376955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1832T>C |
| AA Mutation | p.Met611Thr(p.M611T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320816 |
| Start | 39388839:39388839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584C>T |
| AA Mutation | p.Ala195Val(p.A195V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320816 |
| Start | 39383185:39383185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759729043 |
| CDS Mutation | c.774C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320816 |
| Start | 39382774:39382774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781429014 |
| CDS Mutation | c.1185G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |