Primary Site >> Stomach Cancer
Gene >> AARS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261772 |
| Start | 70258084:70258084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2126A>G |
| AA Mutation | p.Asp709Gly(p.D709G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261772 |
| Start | 70276561:70276561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.404T>C |
| AA Mutation | p.Val135Ala(p.V135A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261772 |
| Start | 70268356:70268356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267606621 |
| CDS Mutation | c.986G>A |
| AA Mutation | p.Arg329His(p.R329H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261772 |
| Start | 70277069:70277069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230G>A |
| AA Mutation | p.Arg77Gln(p.R77Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261772 |
| Start | 70261088:70261088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762734676 |
| CDS Mutation | c.1741G>A |
| AA Mutation | p.Gly581Ser(p.G581S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70268301:70268301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1041T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70252877:70252877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183076680 |
| CDS Mutation | c.2751C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70270301:70270301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.711C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70271831:70271831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147424208 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70255818:70255818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2196T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261772 |
| Start | 70259183:70259183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1789C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261772 |
| Start | 70261124:70261124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747434741 |
| CDS Mutation | c.1705C>T |
| AA Mutation | p.Arg569Ter(p.R569*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |