Primary Site >> Stomach Cancer
Gene >> PTP4A3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329397 |
| Start | 141425081:141425081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776517948 |
| CDS Mutation | c.139C>T |
| AA Mutation | p.Arg47Cys(p.R47C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329397 |
| Start | 141430998:141430998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754768750 |
| CDS Mutation | c.476G>A |
| AA Mutation | p.Arg159Gln(p.R159Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329397 |
| Start | 141430950:141430950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.428G>A |
| AA Mutation | p.Ser143Asn(p.S143N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000329397 |
| Start | 141422293:141422293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.53G>A |
| AA Mutation | p.Arg18His(p.R18H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329397 |
| Start | 141422327:141422327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.87G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329397 |
| Start | 141431017:141431017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145258592 |
| CDS Mutation | c.495G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000329397 |
| Start | 141427049:141427049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000329397 |
| Start | 141426963:141426963(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.227delC |
| AA Mutation | p.Pro76ArgfsTer5(p.P76Rfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |