Primary Site >> Esophagus Cancer
Gene >> ERBB4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211722398:211722398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Cys293Tyr(p.C293Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211665431:211665431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1763A>G |
| AA Mutation | p.Asn588Ser(p.N588S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211623985:211623985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2139G>T |
| AA Mutation | p.Leu713Phe(p.L713F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211947498:211947498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353C>A |
| AA Mutation | p.Ala118Glu(p.A118E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 212538521:212538521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10G>A |
| AA Mutation | p.Ala4Thr(p.A4T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211701994:211701994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1462C>T |
| AA Mutation | p.Arg488Trp(p.R488W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211619266:211619266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2212G>T |
| AA Mutation | p.Val738Leu(p.V738L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000342788 |
| Start | 211702166:211702166(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1290T>G |
| AA Mutation | p.Ser430Arg(p.S430R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 211702110:211702110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1346C>A |
| AA Mutation | p.Ser449Tyr(p.S449Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342788 |
| Start | 212124768:212124768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774895831 |
| CDS Mutation | c.218A>G |
| AA Mutation | p.Asp73Gly(p.D73G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342788 |
| Start | 211750658:211750658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.603A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342788 |
| Start | 211665433:211665433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1761A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342788 |
| Start | 211386908:211386908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3426A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342788 |
| Start | 211383630:211383630(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3912delG |
| AA Mutation | p.Asn1305IlefsTer57(p.N1305Ifs*57) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342788 |
| Start | 211386938:211386938(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3396delC |
| AA Mutation | p.Thr1133ProfsTer19(p.T1133Pfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |