Primary Site >> Stomach Cancer
Gene >> IARS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220100496:220100496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.397A>G |
| AA Mutation | p.Lys133Glu(p.K133E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220105987:220105987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373578830 |
| CDS Mutation | c.1163C>T |
| AA Mutation | p.Thr388Met(p.T388M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220106031:220106031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201122237 |
| CDS Mutation | c.1207G>A |
| AA Mutation | p.Gly403Ser(p.G403S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220140226:220140226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2351G>C |
| AA Mutation | p.Arg784Pro(p.R784P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220143064:220143064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2681C>A |
| AA Mutation | p.Pro894His(p.P894H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220147505:220147505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2909G>T |
| AA Mutation | p.Arg970Leu(p.R970L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220137981:220137981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2113G>T |
| AA Mutation | p.Val705Phe(p.V705F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220105915:220105915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091G>A |
| AA Mutation | p.Cys364Tyr(p.C364Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220102260:220102260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.682T>C |
| AA Mutation | p.Tyr228His(p.Y228H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220141907:220141907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2519A>G |
| AA Mutation | p.His840Arg(p.H840R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220103515:220103515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1019T>C |
| AA Mutation | p.Val340Ala(p.V340A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220126811:220126811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760151453 |
| CDS Mutation | c.1805A>T |
| AA Mutation | p.Asp602Val(p.D602V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366922 |
| Start | 220125320:220125320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1724C>G |
| AA Mutation | p.Pro575Arg(p.P575R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366922 |
| Start | 220145517:220145517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2760G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366922 |
| Start | 220126767:220126767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366922 |
| Start | 220096193:220096193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778652260 |
| CDS Mutation | c.357C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366922 |
| Start | 220107108:220107108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749150836 |
| CDS Mutation | c.1284T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366922 |
| Start | 220142992:220142992(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2610delG |
| AA Mutation | p.Trp870Ter(p.W870*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000366922 |
| Start | 220110939:220110939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1479+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |