Primary Site >> Stomach Cancer
Gene >> JUP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41767506:41767506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.782A>C |
| AA Mutation | p.Lys261Thr(p.K261T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41767542:41767542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377612199;rs786205277 |
| CDS Mutation | c.746C>T |
| AA Mutation | p.Thr249Met(p.T249M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41764771:41764771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782067441 |
| CDS Mutation | c.1100G>A |
| AA Mutation | p.Arg367His(p.R367H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41765031:41765031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782285849 |
| CDS Mutation | c.946G>A |
| AA Mutation | p.Val316Met(p.V316M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41765034:41765034(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.943C>T |
| AA Mutation | p.Leu315Phe(p.L315F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41763102:41763102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782575391 |
| CDS Mutation | c.1378C>T |
| AA Mutation | p.Arg460Cys(p.R460C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41763263:41763263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782188536 |
| CDS Mutation | c.1217A>G |
| AA Mutation | p.Asn406Ser(p.N406S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41769117:41769117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Ala187Thr(p.A187T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41769450:41769450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146581757 |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Glu146Lys(p.E146K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41767494:41767494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782440692 |
| CDS Mutation | c.794G>A |
| AA Mutation | p.Arg265His(p.R265H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41769191:41769191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369121094 |
| CDS Mutation | c.485C>T |
| AA Mutation | p.Ala162Val(p.A162V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41757482:41757482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1979A>G |
| AA Mutation | p.Tyr660Cys(p.Y660C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310706 |
| Start | 41769635:41769635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782061304 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Arg84Gln(p.R84Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |