Primary Site >> Stomach Cancer
Gene >> ZFR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32417731:32417731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482A>T |
| AA Mutation | p.Tyr161Phe(p.Y161F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32397253:32397253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1799A>G |
| AA Mutation | p.His600Arg(p.H600R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32403943:32403943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1187C>T |
| AA Mutation | p.Ala396Val(p.A396V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32388571:32388571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2246C>A |
| AA Mutation | p.Ser749Tyr(p.S749Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32420024:32420024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217G>T |
| AA Mutation | p.Ala73Ser(p.A73S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32355827:32355827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773174560 |
| CDS Mutation | c.3158A>G |
| AA Mutation | p.Asp1053Gly(p.D1053G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32395178:32395178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1960C>T |
| AA Mutation | p.Arg654Cys(p.R654C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32400059:32400059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1661T>C |
| AA Mutation | p.Leu554Pro(p.L554P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32403249:32403249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1373C>T |
| AA Mutation | p.Thr458Met(p.T458M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32379170:32379170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2780G>A |
| AA Mutation | p.Arg927His(p.R927H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32390393:32390393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2024A>G |
| AA Mutation | p.Gln675Arg(p.Q675R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265069 |
| Start | 32380109:32380109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2705C>T |
| AA Mutation | p.Ala902Val(p.A902V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32385590:32385590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2559G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32388546:32388546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771703944 |
| CDS Mutation | c.2271C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32406879:32406879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.927T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32387672:32387672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2376A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32419848:32419848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763164605 |
| CDS Mutation | c.393A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265069 |
| Start | 32380141:32380141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751371575 |
| CDS Mutation | c.2673G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265069 |
| Start | 32404056:32404056(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751974853 |
| CDS Mutation | c.1074delA |
| AA Mutation | p.Glu359LysfsTer4(p.E359Kfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265069 |
| Start | 32355787:32355787(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3198delA |
| AA Mutation | p.Asp1067ThrfsTer13(p.D1067Tfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265069 |
| Start | 32403377:32403377(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1245delA |
| AA Mutation | p.Lys415AsnfsTer42(p.K415Nfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |