Primary Site >> Stomach Cancer
Gene >> JAG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105151704:105151704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1075G>A |
| AA Mutation | p.Gly359Arg(p.G359R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105148427:105148427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2033G>A |
| AA Mutation | p.Cys678Tyr(p.C678Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105146402:105146402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746879958 |
| CDS Mutation | c.2692C>T |
| AA Mutation | p.Arg898Cys(p.R898C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105148364:105148364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373548790 |
| CDS Mutation | c.2096C>T |
| AA Mutation | p.Ala699Val(p.A699V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105168083:105168083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.91G>A |
| AA Mutation | p.Glu31Lys(p.E31K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105143093:105143093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3319C>T |
| AA Mutation | p.Arg1107Cys(p.R1107C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105149275:105149275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1648C>T |
| AA Mutation | p.Arg550Cys(p.R550C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105146689:105146689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781734780 |
| CDS Mutation | c.2515G>A |
| AA Mutation | p.Gly839Arg(p.G839R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105146682:105146682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757271289 |
| CDS Mutation | c.2522C>T |
| AA Mutation | p.Thr841Met(p.T841M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105143580:105143580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3143C>T |
| AA Mutation | p.Ala1048Val(p.A1048V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105148182:105148182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2182T>C |
| AA Mutation | p.Tyr728His(p.Y728H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000331782 |
| Start | 105144932:105144932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773304550 |
| CDS Mutation | c.3082G>A |
| AA Mutation | p.Val1028Met(p.V1028M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000331782 |
| Start | 105155988:105155988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755251181 |
| CDS Mutation | c.477G>T |
| AA Mutation | p.Glu159Asp(p.E159D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105142927:105142927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3485A>G |
| AA Mutation | p.Asp1162Gly(p.D1162G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000331782 |
| Start | 105149286:105149286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754097964 |
| CDS Mutation | c.1637G>A |
| AA Mutation | p.Arg546Gln(p.R546Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105146496:105146496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369469630 |
| CDS Mutation | c.2598C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105155880:105155880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139004148 |
| CDS Mutation | c.585C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105151377:105151377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1173G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105142794:105142794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105148944:105148944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1899C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000331782 |
| Start | 105152180:105152180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138120492 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000331782 |
| Start | 105155580:105155590(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.760_770delGGGGGATGCAC |
| AA Mutation | p.Gly254ArgfsTer18(p.G254Rfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000331782 |
| Start | 105146711:105146712(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2492_2493insAAAAAAGAAAAGCTCCTAAAATCTGC |
| AA Mutation | p.Cys831Ter(p.C831*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |