Primary Site >> Stomach Cancer
Gene >> ITGA6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442250 |
| Start | 172491258:172491258(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2933G>A |
| AA Mutation | p.Cys978Tyr(p.C978Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442250 |
| Start | 172427846:172427846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.58C>A |
| AA Mutation | p.Leu20Ile(p.L20I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442250 |
| Start | 172471019:172471019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689A>C |
| AA Mutation | p.Asn230Thr(p.N230T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000442250 |
| Start | 172469155:172469155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.418C>T |
| AA Mutation | p.His140Tyr(p.H140Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442250 |
| Start | 172472853:172472853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.855T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000442250 |
| Start | 172479725:172479725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747398212 |
| CDS Mutation | c.1590G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000442250 |
| Start | 172471005:172471005(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.681delT |
| AA Mutation | p.Phe227LeufsTer3(p.F227Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000442250 |
| Start | 172475085:172475085(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1265delA |
| AA Mutation | p.Asn422IlefsTer35(p.N422Ifs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000442250 |
| Start | 172472782:172472782(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.788delT |
| AA Mutation | p.Leu263Ter(p.L263*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000442250 |
| Start | 172471004:172471005(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.681dupT |
| AA Mutation | p.Asp228Ter(p.D228*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |