Primary Site >> Stomach Cancer
Gene >> TJP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69225379:69225379(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763855572 |
| CDS Mutation | c.1028A>G |
| AA Mutation | p.Asn343Ser(p.N343S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69221176:69221176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.632G>A |
| AA Mutation | p.Arg211His(p.R211H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69216439:69216439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215G>A |
| AA Mutation | p.Gly72Asp(p.G72D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69234445:69234445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1678A>G |
| AA Mutation | p.Thr560Ala(p.T560A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69238769:69238769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145368713 |
| CDS Mutation | c.2335G>A |
| AA Mutation | p.Val779Met(p.V779M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69212581:69212581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776190114 |
| CDS Mutation | c.94T>C |
| AA Mutation | p.Tyr32His(p.Y32H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69237911:69237911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2213C>G |
| AA Mutation | p.Pro738Arg(p.P738R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69240042:69240042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2461G>A |
| AA Mutation | p.Val821Ile(p.V821I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69254301:69254301(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370985421 |
| CDS Mutation | c.3500G>A |
| AA Mutation | p.Arg1167His(p.R1167H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69216385:69216385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.161A>C |
| AA Mutation | p.Asn54Thr(p.N54T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000377245 |
| Start | 69251364:69251364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3321G>T |
| AA Mutation | p.Arg1107Ser(p.R1107S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69212551:69212551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.64C>A |
| AA Mutation | p.Pro22Thr(p.P22T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377245 |
| Start | 69248135:69248135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139276234 |
| CDS Mutation | c.2791G>A |
| AA Mutation | p.Ala931Thr(p.A931T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377245 |
| Start | 69216437:69216437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780781603 |
| CDS Mutation | c.213G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377245 |
| Start | 69248192:69248210(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2848_2866delACCCGCTCCTCGGAGCCGG |
| AA Mutation | p.Thr950CysfsTer7(p.T950Cfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000377245 |
| Start | 69240013:69240013(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776869985 |
| CDS Mutation | c.2438delT |
| AA Mutation | p.Phe813SerfsTer12(p.F813Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |