Primary Site >> Stomach Cancer
Gene >> STARD8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68721549:68721549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2022T>A |
| AA Mutation | p.Asp674Glu(p.D674E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68716383:68716383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9G>C |
| AA Mutation | p.Leu3Phe(p.L3F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68722073:68722073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2246G>A |
| AA Mutation | p.Gly749Asp(p.G749D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68721671:68721671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2144C>T |
| AA Mutation | p.Ala715Val(p.A715V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68720370:68720370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1756C>T |
| AA Mutation | p.Pro586Ser(p.P586S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68721107:68721107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1993C>A |
| AA Mutation | p.Leu665Ile(p.L665I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68721574:68721574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778278900 |
| CDS Mutation | c.2047G>A |
| AA Mutation | p.Ala683Thr(p.A683T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68719304:68719304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1555G>A |
| AA Mutation | p.Ala519Thr(p.A519T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68717416:68717416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149322857 |
| CDS Mutation | c.262G>A |
| AA Mutation | p.Glu88Lys(p.E88K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68722109:68722109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2282C>T |
| AA Mutation | p.Ala761Val(p.A761V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000252336 |
| Start | 68722611:68722611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2524C>T |
| AA Mutation | p.Pro842Ser(p.P842S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252336 |
| Start | 68718591:68718591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774544532 |
| CDS Mutation | c.1437C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000252336 |
| Start | 68721010:68721010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775110900 |
| CDS Mutation | c.1896C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000252336 |
| Start | 68724094:68724095(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2934_2935dupCA |
| AA Mutation | p.Ile979ThrfsTer69(p.I979Tfs*69) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |