Primary Site >> Stomach Cancer
Gene >> ERF
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249609:42249609(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Ser168Phe(p.S168F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42250431:42250431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.157G>A |
| AA Mutation | p.Gly53Arg(p.G53R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42248589:42248589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1523G>T |
| AA Mutation | p.Gly508Val(p.G508V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249537:42249537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.575G>A |
| AA Mutation | p.Gly192Asp(p.G192D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249669:42249669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755151370 |
| CDS Mutation | c.443C>T |
| AA Mutation | p.Thr148Met(p.T148M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42248656:42248656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1456C>T |
| AA Mutation | p.Arg486Trp(p.R486W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249186:42249186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.926A>G |
| AA Mutation | p.Asp309Gly(p.D309G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249273:42249273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.839C>T |
| AA Mutation | p.Ser280Leu(p.S280L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249188:42249188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.924G>T |
| AA Mutation | p.Glu308Asp(p.E308D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249200:42249200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.912C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249017:42249017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577264310 |
| CDS Mutation | c.1095G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249233:42249233(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.879delG |
| AA Mutation | p.Ser295AlafsTer16(p.S295Afs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000222329 |
| Start | 42249216:42249216(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs780487406 |
| CDS Mutation | c.896delG |
| AA Mutation | p.Gly299GlufsTer12(p.G299Efs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000222329 |
| Start | 42250498:42250498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.90G>A |
| AA Mutation | p.Trp30Ter(p.W30*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |