Primary Site >> Stomach Cancer
Gene >> JAK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64847572:64847572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1859T>C |
| AA Mutation | p.Ile620Thr(p.I620T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64844111:64844111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2356A>T |
| AA Mutation | p.Ile786Phe(p.I786F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64866979:64866979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.877A>T |
| AA Mutation | p.Ile293Phe(p.I293F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64838068:64838068(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3004C>T |
| AA Mutation | p.Arg1002Trp(p.R1002W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000342505 |
| Start | 64835396:64835396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3369G>T |
| AA Mutation | p.Glu1123Asp(p.E1123D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64869353:64869353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605T>C |
| AA Mutation | p.Met202Thr(p.M202T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64844197:64844197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2270C>T |
| AA Mutation | p.Pro757Leu(p.P757L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64836187:64836187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3169A>G |
| AA Mutation | p.Lys1057Glu(p.K1057E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342505 |
| Start | 64855533:64855533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1624C>T |
| AA Mutation | p.Arg542Cys(p.R542C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64857680:64857680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs55788790 |
| CDS Mutation | c.1434C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64841572:64841572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2433G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64869397:64869397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777770696 |
| CDS Mutation | c.561C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64847598:64847598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1833T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64857740:64857740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762097420 |
| CDS Mutation | c.1374C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64838501:64838501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2931C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342505 |
| Start | 64879108:64879108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374624103 |
| CDS Mutation | c.246C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64873428:64873428(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.425delA |
| AA Mutation | p.Lys142ArgfsTer26(p.K142Rfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64841314:64841314(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2580delA |
| AA Mutation | p.Lys860AsnfsTer16(p.K860Nfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64864947:64864947(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1016delA |
| AA Mutation | p.Asn339IlefsTer3(p.N339Ifs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64845610:64845610(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2018delG |
| AA Mutation | p.Gly673ValfsTer30(p.G673Vfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64860150:64860150(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs777215086 |
| CDS Mutation | c.1289delC |
| AA Mutation | p.Pro430ArgfsTer2(p.P430Rfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64835459:64835460(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3301_3305dupGTCAC |
| AA Mutation | p.Arg1103SerfsTer5(p.R1103Sfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64873427:64873428(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.425dupA |
| AA Mutation | p.Ile143AspfsTer9(p.I143Dfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342505 |
| Start | 64860149:64860150(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs755650243 |
| CDS Mutation | c.1289dupC |
| AA Mutation | p.Leu431ValfsTer22(p.L431Vfs*22) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |