Primary Site >> Pancreatic Cancer
Gene >> MYLK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123626924:123626924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374662467 |
| CDS Mutation | c.5132C>T |
| AA Mutation | p.Thr1711Met(p.T1711M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123700073:123700073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202025561 |
| CDS Mutation | c.3395C>T |
| AA Mutation | p.Thr1132Met(p.T1132M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123620276:123620276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5299C>A |
| AA Mutation | p.Leu1767Ile(p.L1767I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123629495:123629495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5093A>C |
| AA Mutation | p.Asn1698Thr(p.N1698T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123649004:123649004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4382C>T |
| AA Mutation | p.Ser1461Phe(p.S1461F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123692764:123692764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189757903 |
| CDS Mutation | c.3536C>T |
| AA Mutation | p.Ala1179Val(p.A1179V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123708739:123708739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2099G>A |
| AA Mutation | p.Ser700Asn(p.S700N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123733974:123733974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1022C>A |
| AA Mutation | p.Thr341Asn(p.T341N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000360304 |
| Start | 123700383:123700383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3085G>A |
| AA Mutation | p.Ala1029Thr(p.A1029T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123664190:123664190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563116446 |
| CDS Mutation | c.3900G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123692811:123692811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3489G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123666300:123666300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201873975 |
| CDS Mutation | c.3750C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000360304 |
| Start | 123618745:123618745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5394G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |