Primary Site >> Stomach Cancer
Gene >> WLS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000354777 |
| Start | 68098701:68098701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1563A>C |
| AA Mutation | p.Glu521Asp(p.E521D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262348 |
| Start | 68150346:68150346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373658553 |
| CDS Mutation | c.814G>A |
| AA Mutation | p.Ala272Thr(p.A272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262348 |
| Start | 68145886:68145886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1261C>G |
| AA Mutation | p.Arg421Gly(p.R421G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262348 |
| Start | 68150199:68150199(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.961G>A |
| AA Mutation | p.Glu321Lys(p.E321K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262348 |
| Start | 68194060:68194060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.274T>G |
| AA Mutation | p.Phe92Val(p.F92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262348 |
| Start | 68194007:68194007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.327C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262348 |
| Start | 68137907:68137907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs537667082 |
| CDS Mutation | c.1389C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262348 |
| Start | 68137875:68137875(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1421delT |
| AA Mutation | p.Phe474SerfsTer15(p.F474Sfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000354777 |
| Start | 68098695:68098695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764307335 |
| CDS Mutation | c.1569T>A |
| AA Mutation | p.Tyr523Ter(p.Y523*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |