Primary Site >> Esophagus Cancer
Gene >> MYH7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417249:23417249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139646545 |
| CDS Mutation | c.4423C>T |
| AA Mutation | p.Arg1475Cys(p.R1475C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23422231:23422231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3194G>T |
| AA Mutation | p.Ser1065Ile(p.S1065I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23425971:23425971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913637 |
| CDS Mutation | c.2155C>T |
| AA Mutation | p.Arg719Trp(p.R719W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23424832:23424832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2616G>T |
| AA Mutation | p.Glu872Asp(p.E872D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417508:23417508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397516211 |
| CDS Mutation | c.4348G>A |
| AA Mutation | p.Asp1450Asn(p.D1450N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23417234:23417234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4438G>C |
| AA Mutation | p.Glu1480Gln(p.E1480Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416197:23416197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4760A>C |
| AA Mutation | p.Lys1587Thr(p.K1587T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23420070:23420070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3501C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23416183:23416183(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4774C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355349 |
| Start | 23421021:23421021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200664031 |
| CDS Mutation | c.3273C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |