Primary Site >> Stomach Cancer
Gene >> PTPN3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109445255:109445255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.451T>A |
| AA Mutation | p.Ser151Thr(p.S151T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109404497:109404497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1904C>T |
| AA Mutation | p.Ala635Val(p.A635V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109436926:109436926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193920798 |
| CDS Mutation | c.632C>T |
| AA Mutation | p.Ala211Val(p.A211V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109454562:109454562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302G>A |
| AA Mutation | p.Cys101Tyr(p.C101Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109381746:109381746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370374314 |
| CDS Mutation | c.2570C>T |
| AA Mutation | p.Thr857Ile(p.T857I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109379593:109379593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780087068 |
| CDS Mutation | c.2705A>G |
| AA Mutation | p.Tyr902Cys(p.Y902C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109381675:109381675(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2641C>T |
| AA Mutation | p.Arg881Cys(p.R881C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109406507:109406507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1747C>T |
| AA Mutation | p.Arg583Trp(p.R583W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000374541 |
| Start | 109448811:109448811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.413G>T |
| AA Mutation | p.Arg138Met(p.R138M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374541 |
| Start | 109382408:109382408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2422G>A |
| AA Mutation | p.Ala808Thr(p.A808T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109381769:109381769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749013475 |
| CDS Mutation | c.2547C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109438137:109438137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148263399 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109410265:109410265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1464C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109457177:109457177(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109454515:109454515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.349C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109404472:109404472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1929C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374541 |
| Start | 109445256:109445256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150667989 |
| CDS Mutation | c.450G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374541 |
| Start | 109391494:109391494(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2021delA |
| AA Mutation | p.Asn674ThrfsTer28(p.N674Tfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000374541 |
| Start | 109381684:109381684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201209437 |
| CDS Mutation | c.2632C>T |
| AA Mutation | p.Arg878Ter(p.R878*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |