Primary Site >> Stomach Cancer
Gene >> ABCC11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48214991:48214991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552749952 |
| CDS Mutation | c.1138G>A |
| AA Mutation | p.Gly380Arg(p.G380R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48215323:48215323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.973G>A |
| AA Mutation | p.Val325Met(p.V325M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48200299:48200299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs16945928 |
| CDS Mutation | c.2059G>A |
| AA Mutation | p.Val687Ile(p.V687I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48222749:48222749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.626T>C |
| AA Mutation | p.Leu209Pro(p.L209P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48198006:48198006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2279C>T |
| AA Mutation | p.Ala760Val(p.A760V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48192704:48192704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765218887 |
| CDS Mutation | c.2522G>A |
| AA Mutation | p.Arg841Gln(p.R841Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48231846:48231846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.76G>T |
| AA Mutation | p.Asp26Tyr(p.D26Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48227848:48227848(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353C>A |
| AA Mutation | p.Pro118His(p.P118H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48200421:48200421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774404726 |
| CDS Mutation | c.1937G>A |
| AA Mutation | p.Arg646His(p.R646H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48167312:48167312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139034695 |
| CDS Mutation | c.4111G>A |
| AA Mutation | p.Ala1371Thr(p.A1371T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48213474:48213474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148839428 |
| CDS Mutation | c.1325C>T |
| AA Mutation | p.Thr442Met(p.T442M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48224425:48224425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779714888 |
| CDS Mutation | c.400C>T |
| AA Mutation | p.His134Tyr(p.H134Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48216230:48216230(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.835C>T |
| AA Mutation | p.Pro279Ser(p.P279S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48205488:48205488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1730T>C |
| AA Mutation | p.Val577Ala(p.V577A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48167636:48167636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3916G>T |
| AA Mutation | p.Ala1306Ser(p.A1306S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356608 |
| Start | 48216209:48216209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200134154 |
| CDS Mutation | c.856G>A |
| AA Mutation | p.Ala286Thr(p.A286T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48178612:48178612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3333A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48215312:48215312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.984G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48177063:48177063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3399G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48192628:48192628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745928898 |
| CDS Mutation | c.2598C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48176943:48176943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370633599 |
| CDS Mutation | c.3519C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356608 |
| Start | 48193882:48193882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2505G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356608 |
| Start | 48227951:48227951(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.250delC |
| AA Mutation | p.Gln84SerfsTer21(p.Q84Sfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000356608 |
| Start | 48192575:48192575(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2651delT |
| AA Mutation | p.Phe884SerfsTer25(p.F884Sfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000356608 |
| Start | 48192705:48192705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752713916 |
| CDS Mutation | c.2521C>T |
| AA Mutation | p.Arg841Ter(p.R841*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |