Primary Site >> Stomach Cancer
Gene >> STK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419617 |
| Start | 98749310:98749310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.317C>T |
| AA Mutation | p.Ser106Phe(p.S106F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419617 |
| Start | 98749326:98749326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301T>C |
| AA Mutation | p.Tyr101His(p.Y101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419617 |
| Start | 98455966:98455966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770553429 |
| CDS Mutation | c.1352G>A |
| AA Mutation | p.Arg451Gln(p.R451Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419617 |
| Start | 98749317:98749317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.310G>A |
| AA Mutation | p.Ala104Thr(p.A104T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000419617 |
| Start | 98548053:98548053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1057C>A |
| AA Mutation | p.His353Asn(p.H353N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000419617 |
| Start | 98706623:98706623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.528A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000419617 |
| Start | 98749318:98749318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373807046 |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |