Primary Site >> Stomach Cancer
Gene >> EEA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92778101:92778101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3733G>T |
| AA Mutation | p.Ala1245Ser(p.A1245S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92798915:92798915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2944C>T |
| AA Mutation | p.Leu982Phe(p.L982F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92776906:92776906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4051G>A |
| AA Mutation | p.Glu1351Lys(p.E1351K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92787939:92787939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3078A>C |
| AA Mutation | p.Glu1026Asp(p.E1026D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92857324:92857324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.317C>T |
| AA Mutation | p.Ser106Leu(p.S106L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92816374:92816374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1755G>C |
| AA Mutation | p.Lys585Asn(p.K585N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92832533:92832533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1233A>C |
| AA Mutation | p.Gln411His(p.Q411H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322349 |
| Start | 92802664:92802664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2410A>G |
| AA Mutation | p.Lys804Glu(p.K804E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000322349 |
| Start | 92776846:92776846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4111C>T |
| AA Mutation | p.Arg1371Trp(p.R1371W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322349 |
| Start | 92776907:92776907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142495165 |
| CDS Mutation | c.4050C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322349 |
| Start | 92819327:92819327(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1709delA |
| AA Mutation | p.Asn570ThrfsTer8(p.N570Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322349 |
| Start | 92842469:92842469(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.911delA |
| AA Mutation | p.Asn304IlefsTer4(p.N304Ifs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322349 |
| Start | 92779164:92779164(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3605delA |
| AA Mutation | p.Lys1202ArgfsTer6(p.K1202Rfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322349 |
| Start | 92802643:92802643(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776707160 |
| CDS Mutation | c.2431delA |
| AA Mutation | p.Ile811SerfsTer2(p.I811Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |