Primary Site >> Liver Cancer
Gene >> MYOM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3215132:3215132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777908113 |
| CDS Mutation | c.92G>A |
| AA Mutation | p.Arg31Gln(p.R31Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000356443 |
| Start | 3083789:3083789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4484A>T |
| AA Mutation | p.Asn1495Ile(p.N1495I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3129397:3129397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2629A>C |
| AA Mutation | p.Ser877Arg(p.S877R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3067426:3067426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4894A>T |
| AA Mutation | p.Thr1632Ser(p.T1632S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3086132:3086132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4157A>T |
| AA Mutation | p.Glu1386Val(p.E1386V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3090727:3090727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3940G>A |
| AA Mutation | p.Gly1314Arg(p.G1314R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356443 |
| Start | 3100194:3100194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756213299 |
| CDS Mutation | c.3692G>A |
| AA Mutation | p.Arg1231His(p.R1231H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356443 |
| Start | 3134724:3134724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769216946 |
| CDS Mutation | c.2310G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356443 |
| Start | 3155039:3155039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745600639 |
| CDS Mutation | c.1551G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |