Primary Site >> Stomach Cancer
Gene >> BOP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569669 |
| Start | 144265022:144265022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.440T>C |
| AA Mutation | p.Phe147Ser(p.F147S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569669 |
| Start | 144265029:144265029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Asp145Asn(p.D145N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569669 |
| Start | 144264025:144264025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1096C>T |
| AA Mutation | p.Arg366Cys(p.R366C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569669 |
| Start | 144264528:144264528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.752T>C |
| AA Mutation | p.Val251Ala(p.V251A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000569669 |
| Start | 144289265:144289265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549552930 |
| CDS Mutation | c.139G>A |
| AA Mutation | p.Gly47Ser(p.G47S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569669 |
| Start | 144264264:144264264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.939G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569669 |
| Start | 144264590:144264590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569669 |
| Start | 144289140:144289140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199980866 |
| CDS Mutation | c.264C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000569669 |
| Start | 144289179:144289179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138704768 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569669 |
| Start | 144289298:144289298(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs782769521 |
| CDS Mutation | c.106delC |
| AA Mutation | p.Leu36SerfsTer154(p.L36Sfs*154) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569669 |
| Start | 144263299:144263299(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1527delC |
| AA Mutation | p.Leu510CysfsTer28(p.L510Cfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000569669 |
| Start | 144265038:144265038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.424G>T |
| AA Mutation | p.Glu142Ter(p.E142*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000569669 |
| Start | 144263537:144263538(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1364dupG |
| AA Mutation | p.Val456ArgfsTer51(p.V456Rfs*51) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |