Primary Site >> Stomach Cancer
Gene >> DYNC1I2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397119 |
| Start | 171728381:171728381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1220T>A |
| AA Mutation | p.Ile407Asn(p.I407N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397119 |
| Start | 171726843:171726843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.923A>C |
| AA Mutation | p.Glu308Ala(p.E308A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397119 |
| Start | 171727832:171727832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1008G>A |
| AA Mutation | p.Met336Ile(p.M336I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397119 |
| Start | 171728355:171728355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1194G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397119 |
| Start | 171690209:171690209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.54G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397119 |
| Start | 171707363:171707363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753569691 |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397119 |
| Start | 171707324:171707324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.282C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000397119 |
| Start | 171692829:171692830(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.168_169delAA |
| AA Mutation | p.Arg57GlufsTer4(p.R57Efs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000397119 |
| Start | 171706546:171706547(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs749854400 |
| CDS Mutation | c.232dupT |
| AA Mutation | p.Ser78PhefsTer2(p.S78Ffs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |