Primary Site >> Stomach Cancer
Gene >> IGFBP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275525 |
| Start | 45888744:45888744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.92C>T |
| AA Mutation | p.Ala31Val(p.A31V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275525 |
| Start | 45888709:45888709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57G>T |
| AA Mutation | p.Gln19His(p.Q19H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275525 |
| Start | 45891974:45891974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.562G>T |
| AA Mutation | p.Ala188Ser(p.A188S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275525 |
| Start | 45890622:45890622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Ala142Thr(p.A142T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275525 |
| Start | 45891940:45891940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.528C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275525 |
| Start | 45888679:45888679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.27C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000275525 |
| Start | 45890706:45890706(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.513delA |
| AA Mutation | p.Lys171AsnfsTer8(p.K171Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000275525 |
| Start | 45891941:45891941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776233561 |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Arg177Ter(p.R177*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |