Primary Site >> Stomach Cancer
Gene >> PITX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265340 |
| Start | 135028907:135028907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817G>A |
| AA Mutation | p.Val273Ile(p.V273I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265340 |
| Start | 135028979:135028979(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.745A>G |
| AA Mutation | p.Thr249Ala(p.T249A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265340 |
| Start | 135028799:135028799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140746945 |
| CDS Mutation | c.925G>A |
| AA Mutation | p.Ala309Thr(p.A309T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265340 |
| Start | 135028951:135028951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.773C>T |
| AA Mutation | p.Ser258Leu(p.S258L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265340 |
| Start | 135029025:135029025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.699C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265340 |
| Start | 135029004:135029004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.720G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265340 |
| Start | 135031285:135031285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766860676 |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265340 |
| Start | 135029288:135029289(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.435dupT |
| AA Mutation | p.Lys146Ter(p.K146*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |