Primary Site >> Stomach Cancer
Gene >> DAB2IP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121782472:121782472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765169272 |
| CDS Mutation | c.3544G>A |
| AA Mutation | p.Glu1182Lys(p.E1182K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121781544:121781544(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3395A>G |
| AA Mutation | p.Asp1132Gly(p.D1132G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121782386:121782386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3458C>T |
| AA Mutation | p.Thr1153Ile(p.T1153I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121757092:121757092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.442G>A |
| AA Mutation | p.Asp148Asn(p.D148N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772791:121772791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761339512 |
| CDS Mutation | c.2263C>T |
| AA Mutation | p.Arg755Cys(p.R755C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772885:121772885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780248582 |
| CDS Mutation | c.2357C>T |
| AA Mutation | p.Pro786Leu(p.P786L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772830:121772830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302G>A |
| AA Mutation | p.Asp768Asn(p.D768N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121773323:121773323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2795G>A |
| AA Mutation | p.Arg932His(p.R932H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121763619:121763619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1285G>T |
| AA Mutation | p.Val429Leu(p.V429L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772921:121772921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2393C>G |
| AA Mutation | p.Ala798Gly(p.A798G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121766660:121766660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1627C>T |
| AA Mutation | p.Pro543Ser(p.P543S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121782367:121782367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3439C>T |
| AA Mutation | p.Arg1147Cys(p.R1147C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121760074:121760074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759742711 |
| CDS Mutation | c.805C>T |
| AA Mutation | p.Arg269Cys(p.R269C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000408936 |
| Start | 121766589:121766589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1556C>T |
| AA Mutation | p.Ala519Val(p.A519V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772973:121772973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144586865 |
| CDS Mutation | c.2445C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772982:121772982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2454C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772787:121772787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760694146 |
| CDS Mutation | c.2259C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772976:121772976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777515218 |
| CDS Mutation | c.2448G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121770690:121770690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs535102113 |
| CDS Mutation | c.2044C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121678766:121678766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182778593 |
| CDS Mutation | c.213G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121757055:121757055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.405G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121768519:121768519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1785C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121772952:121772952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2424C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121781515:121781515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533653042 |
| CDS Mutation | c.3366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121770659:121770659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371535507 |
| CDS Mutation | c.2013G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000408936 |
| Start | 121763775:121763775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778950978 |
| CDS Mutation | c.1356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000408936 |
| Start | 121678782:121678782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.228+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | inframe_deletion;splice_region_variant |
| Transcription ID | ENST00000408936 |
| Start | 121781466:121781468(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3319_3321delATG |
| AA Mutation | p.Met1107del(p.M1107del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |