Primary Site >> Esophagus Cancer
Gene >> MYH14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50281697:50281697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4271G>A |
| AA Mutation | p.Arg1424His(p.R1424H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50268302:50268302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2845G>A |
| AA Mutation | p.Gly949Ser(p.G949S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50217708:50217708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759687206 |
| CDS Mutation | c.499C>T |
| AA Mutation | p.Arg167Cys(p.R167C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50281779:50281779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4353G>A |
| AA Mutation | p.Met1451Ile(p.M1451I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50280092:50280092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727504915 |
| CDS Mutation | c.3965G>A |
| AA Mutation | p.Arg1322His(p.R1322H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50280313:50280313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs553162373 |
| CDS Mutation | c.4097G>A |
| AA Mutation | p.Arg1366His(p.R1366H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376970 |
| Start | 50280062:50280062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561525083 |
| CDS Mutation | c.3935C>T |
| AA Mutation | p.Ala1312Val(p.A1312V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376970 |
| Start | 50261504:50261504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2331C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |