Primary Site >> Pancreatic Cancer
Gene >> ITGA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52849374:52849374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759463731 |
| CDS Mutation | c.71G>A |
| AA Mutation | p.Arg24His(p.R24H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52864783:52864783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Val106Ile(p.V106I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52918742:52918742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1999G>A |
| AA Mutation | p.Val667Met(p.V667M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52922850:52922850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2366T>G |
| AA Mutation | p.Val789Gly(p.V789G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52944964:52944964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3307C>A |
| AA Mutation | p.Leu1103Ile(p.L1103I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282588 |
| Start | 52939594:52939594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3083C>T |
| AA Mutation | p.Ala1028Val(p.A1028V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282588 |
| Start | 52933951:52933951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2919T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000282588 |
| Start | 52925470:52925471(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2602dupT |
| AA Mutation | p.Ser868PhefsTer4(p.S868Ffs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |