Primary Site >> Stomach Cancer
Gene >> ITGB5
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000296181 |
| Start | 124773910:124773910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1696C>A |
| AA Mutation | p.His566Asn(p.H566N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124766292:124766292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762359769 |
| CDS Mutation | c.2071G>A |
| AA Mutation | p.Val691Ile(p.V691I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124848456:124848456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.464A>G |
| AA Mutation | p.Asp155Gly(p.D155G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124796455:124796455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1626G>T |
| AA Mutation | p.Lys542Asn(p.K542N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124796484:124796484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1597T>A |
| AA Mutation | p.Cys533Ser(p.C533S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124809078:124809078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1207G>T |
| AA Mutation | p.Asp403Tyr(p.D403Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296181 |
| Start | 124773824:124773824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1782C>G |
| AA Mutation | p.Cys594Trp(p.C594W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124796419:124796419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1662C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124859420:124859420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.183C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124773863:124773863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374962668 |
| CDS Mutation | c.1743C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124841425:124841425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296181 |
| Start | 124796587:124796587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151072606 |
| CDS Mutation | c.1494C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |