Primary Site >> Stomach Cancer
Gene >> EGF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109964515:109964515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1553A>T |
| AA Mutation | p.Asp518Val(p.D518V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109963202:109963202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1342A>G |
| AA Mutation | p.Ser448Gly(p.S448G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109987791:109987791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2539A>G |
| AA Mutation | p.Ile847Val(p.I847V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109943970:109943970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373552129 |
| CDS Mutation | c.638G>A |
| AA Mutation | p.Arg213Gln(p.R213Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109941078:109941078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.260G>T |
| AA Mutation | p.Arg87Ile(p.R87I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109976135:109976135(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1953C>A |
| AA Mutation | p.Phe651Leu(p.F651L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 110004540:110004540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3209C>A |
| AA Mutation | p.Pro1070His(p.P1070H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109976200:109976200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2018G>A |
| AA Mutation | p.Gly673Asp(p.G673D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109987819:109987819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745691794 |
| CDS Mutation | c.2567A>G |
| AA Mutation | p.Gln856Arg(p.Q856R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109945107:109945107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757131048 |
| CDS Mutation | c.772C>T |
| AA Mutation | p.Arg258Cys(p.R258C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109960909:109960909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1109G>A |
| AA Mutation | p.Gly370Glu(p.G370E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265171 |
| Start | 109988596:109988596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2621G>A |
| AA Mutation | p.Cys874Tyr(p.C874Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109994758:109994758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2883G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109994803:109994803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2928T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109960874:109960874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1074T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109980043:109980043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2125A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109941137:109941137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.319A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109980929:109980929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2325A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265171 |
| Start | 109994752:109994752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2877C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265171 |
| Start | 109999828:109999828(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3160delG |
| AA Mutation | p.Ala1054ProfsTer25(p.A1054Pfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265171 |
| Start | 109988618:109988618(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758373637 |
| CDS Mutation | c.2648delC |
| AA Mutation | p.Pro883LeufsTer67(p.P883Lfs*67) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |