Primary Site >> Stomach Cancer
Gene >> ITGB8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20406159:20406159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751381514 |
| CDS Mutation | c.2011G>A |
| AA Mutation | p.Asp671Asn(p.D671N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20380673:20380673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.643A>C |
| AA Mutation | p.Asn215His(p.N215H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20409696:20409696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2105T>C |
| AA Mutation | p.Leu702Pro(p.L702P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20409879:20409879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2192A>G |
| AA Mutation | p.Lys731Arg(p.K731R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20381736:20381736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811G>C |
| AA Mutation | p.Gly271Arg(p.G271R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20379167:20379167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768194871 |
| CDS Mutation | c.505G>A |
| AA Mutation | p.Val169Ile(p.V169I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20367112:20367112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.314A>G |
| AA Mutation | p.His105Arg(p.H105R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20379206:20379206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147908281 |
| CDS Mutation | c.544C>T |
| AA Mutation | p.Arg182Cys(p.R182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222573 |
| Start | 20409911:20409911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2224G>A |
| AA Mutation | p.Val742Ile(p.V742I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222573 |
| Start | 20398973:20398973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1260A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222573 |
| Start | 20409772:20409772(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2186delA |
| AA Mutation | p.Lys729ArgfsTer4(p.K729Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222573 |
| Start | 20401928:20401931(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1492_1495delAAAT |
| AA Mutation | p.Lys498ValfsTer185(p.K498Vfs*185) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222573 |
| Start | 20331827:20331827(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.27delT |
| AA Mutation | p.Phe9LeufsTer81(p.F9Lfs*81) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000222573 |
| Start | 20404711:20404711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1771C>T |
| AA Mutation | p.Gln591Ter(p.Q591*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222573 |
| Start | 20331826:20331827(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs760028800 |
| CDS Mutation | c.27dupT |
| AA Mutation | p.Thr10TyrfsTer34(p.T10Yfs*34) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000222573 |
| Start | 20394895:20394895(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1057-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |