Primary Site >> Stomach Cancer
Gene >> NTRK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156868157:156868157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.482G>C |
| AA Mutation | p.Arg161Pro(p.R161P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156874984:156874984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1330C>T |
| AA Mutation | p.Arg444Trp(p.R444W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156868124:156868124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.449T>C |
| AA Mutation | p.Leu150Pro(p.L150P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156876101:156876101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374799164 |
| CDS Mutation | c.1523G>A |
| AA Mutation | p.Arg508Gln(p.R508Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156873831:156873831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1049A>C |
| AA Mutation | p.Gln350Pro(p.Q350P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156873707:156873707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Pro309Ser(p.P309S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156871723:156871723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200305545 |
| CDS Mutation | c.818G>A |
| AA Mutation | p.Arg273Gln(p.R273Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156873714:156873714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932C>T |
| AA Mutation | p.Pro311Leu(p.P311L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156866914:156866914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.364C>A |
| AA Mutation | p.Leu122Ile(p.L122I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000524377 |
| Start | 156873743:156873743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369367198 |
| CDS Mutation | c.961G>A |
| AA Mutation | p.Val321Met(p.V321M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000524377 |
| Start | 156864731:156864731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000524377 |
| Start | 156874396:156874396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756623123 |
| CDS Mutation | c.1191G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000524377 |
| Start | 156876516:156876516(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1753delC |
| AA Mutation | p.Leu585CysfsTer73(p.L585Cfs*73) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000524377 |
| Start | 156875009:156875009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764771898 |
| CDS Mutation | c.1354+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |