Primary Site >> Stomach Cancer
Gene >> PTPN11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351677 |
| Start | 112486482:112486482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121918467 |
| CDS Mutation | c.1232C>T |
| AA Mutation | p.Thr411Met(p.T411M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351677 |
| Start | 112453269:112453269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.407T>A |
| AA Mutation | p.Leu136His(p.L136H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351677 |
| Start | 112502167:112502167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1623A>C |
| AA Mutation | p.Glu541Asp(p.E541D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351677 |
| Start | 112489084:112489084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397507546 |
| CDS Mutation | c.1508G>T |
| AA Mutation | p.Gly503Val(p.G503V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351677 |
| Start | 112488466:112488466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121918457 |
| CDS Mutation | c.1403C>T |
| AA Mutation | p.Thr468Met(p.T468M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351677 |
| Start | 112486618:112486618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1368G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351677 |
| Start | 112489043:112489043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs539373294 |
| CDS Mutation | c.1467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351677 |
| Start | 112486492:112486492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351677 |
| Start | 112477934:112477934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371951288 |
| CDS Mutation | c.1011G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000351677 |
| Start | 112478017:112478017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1092+2T>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |