Primary Site >> Stomach Cancer
Gene >> IARS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92278208:92278208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.824T>C |
| AA Mutation | p.Ile275Thr(p.I275T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92247458:92247458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2710C>T |
| AA Mutation | p.Arg904Cys(p.R904C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375643 |
| Start | 92242154:92242154(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3177G>T |
| AA Mutation | p.Gln1059His(p.Q1059H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92247511:92247511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2657A>C |
| AA Mutation | p.Asn886Thr(p.N886T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92250206:92250206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370194547 |
| CDS Mutation | c.2513G>A |
| AA Mutation | p.Arg838Gln(p.R838Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92289364:92289364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.56T>G |
| AA Mutation | p.Leu19Trp(p.L19W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92222592:92222592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3634T>C |
| AA Mutation | p.Tyr1212His(p.Y1212H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92287807:92287807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.380A>T |
| AA Mutation | p.Tyr127Phe(p.Y127F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375643 |
| Start | 92280772:92280772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.719C>T |
| AA Mutation | p.Pro240Leu(p.P240L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375643 |
| Start | 92263010:92263010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1746G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375643 |
| Start | 92268249:92268249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144681367 |
| CDS Mutation | c.1356A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375643 |
| Start | 92245052:92245052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2811C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375643 |
| Start | 92271034:92271034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140292751 |
| CDS Mutation | c.1156C>T |
| AA Mutation | p.Arg386Ter(p.R386*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375643 |
| Start | 92277872:92277872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.885T>A |
| AA Mutation | p.Tyr295Ter(p.Y295*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375643 |
| Start | 92268275:92268275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745932544 |
| CDS Mutation | c.1330C>T |
| AA Mutation | p.Arg444Ter(p.R444*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |