Primary Site >> Stomach Cancer
Gene >> RAG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574286:36574286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.982T>C |
| AA Mutation | p.Cys328Arg(p.C328R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574532:36574532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758288006 |
| CDS Mutation | c.1228C>T |
| AA Mutation | p.Arg410Trp(p.R410W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36576390:36576390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3086T>C |
| AA Mutation | p.Leu1029Ser(p.L1029S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573459:36573459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155C>A |
| AA Mutation | p.Ser52Tyr(p.S52Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574182:36574182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Cys293Tyr(p.C293Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573698:36573698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773742414 |
| CDS Mutation | c.394C>T |
| AA Mutation | p.Pro132Ser(p.P132S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36576256:36576256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2952C>G |
| AA Mutation | p.Cys984Trp(p.C984W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573329:36573329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771932715 |
| CDS Mutation | c.25T>G |
| AA Mutation | p.Leu9Val(p.L9V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36575721:36575721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2417A>G |
| AA Mutation | p.Glu806Gly(p.E806G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574244:36574244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121918568 |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Arg314Trp(p.R314W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573720:36573720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416G>A |
| AA Mutation | p.Gly139Asp(p.G139D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36575314:36575314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769576393 |
| CDS Mutation | c.2010G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573751:36573751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.447T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574288:36574288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.984T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36575449:36575449(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2145G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574507:36574507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753446485 |
| CDS Mutation | c.1203G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36573760:36573760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368797111 |
| CDS Mutation | c.456G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299440 |
| Start | 36575929:36575929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200264827 |
| CDS Mutation | c.2625C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299440 |
| Start | 36574004:36574004(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.705delA |
| AA Mutation | p.Lys235AsnfsTer29(p.K235Nfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000299440 |
| Start | 36576172:36576173(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2872dupG |
| AA Mutation | p.Ala958GlyfsTer5(p.A958Gfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |