Primary Site >> Stomach Cancer
Gene >> ITGA5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54405686:54405686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375602887 |
| CDS Mutation | c.994G>A |
| AA Mutation | p.Ala332Thr(p.A332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54408190:54408190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.737A>G |
| AA Mutation | p.Tyr246Cys(p.Y246C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54402020:54402020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2207C>T |
| AA Mutation | p.Pro736Leu(p.P736L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54419062:54419062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.137C>T |
| AA Mutation | p.Ala46Val(p.A46V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54403260:54403260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1841C>T |
| AA Mutation | p.Pro614Leu(p.P614L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54409343:54409343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.472C>T |
| AA Mutation | p.Pro158Ser(p.P158S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54398601:54398601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145576475 |
| CDS Mutation | c.2939G>A |
| AA Mutation | p.Arg980His(p.R980H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54403659:54403659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770030872 |
| CDS Mutation | c.1742G>A |
| AA Mutation | p.Arg581Gln(p.R581Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54405292:54405292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1099G>A |
| AA Mutation | p.Val367Ile(p.V367I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54419032:54419032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777360125 |
| CDS Mutation | c.167C>T |
| AA Mutation | p.Pro56Leu(p.P56L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54419093:54419093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.106C>T |
| AA Mutation | p.Pro36Ser(p.P36S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54405319:54405319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775846363 |
| CDS Mutation | c.1072C>T |
| AA Mutation | p.Arg358Trp(p.R358W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293379 |
| Start | 54403725:54403725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1676G>A |
| AA Mutation | p.Arg559Gln(p.R559Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293379 |
| Start | 54405323:54405323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774155456 |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |