Primary Site >> Stomach Cancer
Gene >> STYK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075503 |
| Start | 10634046:10634046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.131T>C |
| AA Mutation | p.Ile44Thr(p.I44T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075503 |
| Start | 10624666:10624666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911G>A |
| AA Mutation | p.Ser304Asn(p.S304N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000075503 |
| Start | 10622640:10622640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.965T>C |
| AA Mutation | p.Leu322Pro(p.L322P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075503 |
| Start | 10624675:10624675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.902G>C |
| AA Mutation | p.Arg301Thr(p.R301T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000075503 |
| Start | 10624741:10624741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147511596 |
| CDS Mutation | c.836G>A |
| AA Mutation | p.Arg279Gln(p.R279Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000075503 |
| Start | 10629502:10629502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.624C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000075503 |
| Start | 10629636:10629636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759063099 |
| CDS Mutation | c.490C>T |
| AA Mutation | p.Arg164Ter(p.R164*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |