Primary Site >> Esophagus Cancer
Gene >> MYLK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123733081:123733081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1331A>G |
| AA Mutation | p.Glu444Gly(p.E444G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123700335:123700335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3133G>C |
| AA Mutation | p.Glu1045Gln(p.E1045Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123638138:123638138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4894G>T |
| AA Mutation | p.Val1632Leu(p.V1632L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123700325:123700325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3143A>G |
| AA Mutation | p.Lys1048Arg(p.K1048R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123733948:123733948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532659627 |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Ala350Thr(p.A350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123700165:123700165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3303G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123734195:123734195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.801C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123657145:123657145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574785619 |
| CDS Mutation | c.4269G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |