Primary Site >> Stomach Cancer
Gene >> CEMIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80942022:80942022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3581C>A |
| AA Mutation | p.Pro1194Gln(p.P1194Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80933437:80933437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2986A>G |
| AA Mutation | p.Ile996Val(p.I996V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80895032:80895032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779741917 |
| CDS Mutation | c.1129T>C |
| AA Mutation | p.Tyr377His(p.Y377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80884188:80884188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.631A>G |
| AA Mutation | p.Arg211Gly(p.R211G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80943060:80943060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3815T>C |
| AA Mutation | p.Ile1272Thr(p.I1272T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80895950:80895950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1301A>C |
| AA Mutation | p.Lys434Thr(p.K434T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80948917:80948917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4079A>C |
| AA Mutation | p.Lys1360Thr(p.K1360T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80943026:80943026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768391358 |
| CDS Mutation | c.3781C>T |
| AA Mutation | p.His1261Tyr(p.H1261Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80884209:80884209(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.652C>T |
| AA Mutation | p.Arg218Cys(p.R218C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80884341:80884341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.784C>T |
| AA Mutation | p.His262Tyr(p.H262Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80937853:80937853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750169411 |
| CDS Mutation | c.3281C>T |
| AA Mutation | p.Ser1094Leu(p.S1094L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80896040:80896040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1391C>A |
| AA Mutation | p.Pro464His(p.P464H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80925725:80925725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752233938 |
| CDS Mutation | c.2390G>A |
| AA Mutation | p.Arg797His(p.R797H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80943087:80943087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369847646 |
| CDS Mutation | c.3842C>T |
| AA Mutation | p.Ala1281Val(p.A1281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80948832:80948832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3994C>T |
| AA Mutation | p.Arg1332Trp(p.R1332W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80909196:80909196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147046826 |
| CDS Mutation | c.1687G>A |
| AA Mutation | p.Gly563Ser(p.G563S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80941896:80941896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3455C>A |
| AA Mutation | p.Ala1152Asp(p.A1152D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80942326:80942326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760551866 |
| CDS Mutation | c.3688G>A |
| AA Mutation | p.Ala1230Thr(p.A1230T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80879766:80879766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.292C>T |
| AA Mutation | p.His98Tyr(p.H98Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220244 |
| Start | 80880967:80880967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778020593 |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Ala150Thr(p.A150T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80936850:80936850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745812845 |
| CDS Mutation | c.3186C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80936853:80936853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs79713495 |
| CDS Mutation | c.3189C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80888756:80888756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80889553:80889553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1047T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80921086:80921086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755340760 |
| CDS Mutation | c.2058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220244 |
| Start | 80948810:80948810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754943195 |
| CDS Mutation | c.3972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220244 |
| Start | 80895035:80895035(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1137delA |
| AA Mutation | p.Gly380AlafsTer28(p.G380Afs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220244 |
| Start | 80881053:80881053(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753314096 |
| CDS Mutation | c.540delT |
| AA Mutation | p.Phe180LeufsTer44(p.F180Lfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220244 |
| Start | 80941879:80941880(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3447_3448dupGA |
| AA Mutation | p.Lys1150ArgfsTer8(p.K1150Rfs*8) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |