Primary Site >> Stomach Cancer
Gene >> RABGAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 122984602:122984602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Gly90Ser(p.G90S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123020440:123020440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1775A>G |
| AA Mutation | p.Tyr592Cys(p.Y592C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 122986262:122986262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Val145Ile(p.V145I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123074303:123074303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2128T>C |
| AA Mutation | p.Tyr710His(p.Y710H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123098776:123098776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2795C>A |
| AA Mutation | p.Ser932Tyr(p.S932Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 122997289:122997289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132T>C |
| AA Mutation | p.Ser378Pro(p.S378P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 122998649:122998649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1257G>T |
| AA Mutation | p.Gln419His(p.Q419H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123065375:123065375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144231846 |
| CDS Mutation | c.1822C>T |
| AA Mutation | p.Arg608Trp(p.R608W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123101587:123101587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764209083 |
| CDS Mutation | c.2911C>T |
| AA Mutation | p.Arg971Trp(p.R971W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 122998729:122998729(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752925671 |
| CDS Mutation | c.1337G>A |
| AA Mutation | p.Arg446His(p.R446H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373647 |
| Start | 123076743:123076743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2405A>T |
| AA Mutation | p.Glu802Val(p.E802V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373647 |
| Start | 122986330:122986330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374096472 |
| CDS Mutation | c.501C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373647 |
| Start | 122996545:122996545(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373647 |
| Start | 123101649:123101649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2973T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373647 |
| Start | 122989366:122989366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.660A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 123098763:123098763(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749213218 |
| CDS Mutation | c.2789delA |
| AA Mutation | p.Asn930ThrfsTer15(p.N930Tfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 123101648:123101648(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2975delT |
| AA Mutation | p.Leu992Ter(p.L992*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 122984678:122984678(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.348delA |
| AA Mutation | p.Lys116AsnfsTer4(p.K116Nfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 122997318:122997318(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1164delA |
| AA Mutation | p.Lys388AsnfsTer8(p.K388Nfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 123098763:123098764(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2788_2789delAA |
| AA Mutation | p.Asn930GlnfsTer6(p.N930Qfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000373647 |
| Start | 123098762:123098763(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs768477276 |
| CDS Mutation | c.2789dupA |
| AA Mutation | p.Asn930LysfsTer7(p.N930Kfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |