Primary Site >> Stomach Cancer
Gene >> MARK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103468079:103468079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157A>G |
| AA Mutation | p.Lys386Arg(p.K386R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103475020:103475020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779860437 |
| CDS Mutation | c.1292C>T |
| AA Mutation | p.Ala431Val(p.A431V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103475184:103475184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202148764 |
| CDS Mutation | c.1456C>T |
| AA Mutation | p.Arg486Cys(p.R486C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103405211:103405211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Gly63Ser(p.G63S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103491899:103491899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1709G>A |
| AA Mutation | p.Arg570Gln(p.R570Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103386062:103386062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.33T>G |
| AA Mutation | p.Asn11Lys(p.N11K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000429436 |
| Start | 103475170:103475170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183634888 |
| CDS Mutation | c.1442C>T |
| AA Mutation | p.Ala481Val(p.A481V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000429436 |
| Start | 103405228:103405228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.204A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000429436 |
| Start | 103468119:103468119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1197G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000429436 |
| Start | 103457184:103457184(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.459delA |
| AA Mutation | p.Glu154LysfsTer33(p.E154Kfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000429436 |
| Start | 103491907:103491907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763214749 |
| CDS Mutation | c.1717C>T |
| AA Mutation | p.Arg573Ter(p.R573*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |