Primary Site >> Pancreatic Cancer
Gene >> SYNE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152218326:152218326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.22122A>G |
| AA Mutation | p.Ile7374Met(p.I7374M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152293733:152293733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80265744 |
| CDS Mutation | c.17867G>A |
| AA Mutation | p.Arg5956His(p.R5956H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152136788:152136788(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777390431 |
| CDS Mutation | c.25489G>A |
| AA Mutation | p.Ala8497Thr(p.A8497T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152141220:152141220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.25229C>T |
| AA Mutation | p.Thr8410Ile(p.T8410I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152164300:152164300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23653G>A |
| AA Mutation | p.Val7885Ile(p.V7885I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152176481:152176481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.23540G>T |
| AA Mutation | p.Ser7847Ile(p.S7847I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152256758:152256758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18980G>T |
| AA Mutation | p.Ser6327Ile(p.S6327I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152321312:152321312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16162C>A |
| AA Mutation | p.Leu5388Ile(p.L5388I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152326390:152326390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184360743 |
| CDS Mutation | c.15199G>A |
| AA Mutation | p.Gly5067Ser(p.G5067S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330997:152330997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13688C>A |
| AA Mutation | p.Ser4563Tyr(p.S4563Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152354873:152354873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10712C>T |
| AA Mutation | p.Ala3571Val(p.A3571V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152362219:152362219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10250G>T |
| AA Mutation | p.Arg3417Met(p.R3417M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152373125:152373125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146402274 |
| CDS Mutation | c.9419C>T |
| AA Mutation | p.Ala3140Val(p.A3140V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152385775:152385775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371684437 |
| CDS Mutation | c.8551G>A |
| AA Mutation | p.Glu2851Lys(p.E2851K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416871:152416871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5566G>A |
| AA Mutation | p.Ala1856Thr(p.A1856T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152428210:152428210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4971G>T |
| AA Mutation | p.Trp1657Cys(p.W1657C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152455913:152455913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2700G>T |
| AA Mutation | p.Gln900His(p.Q900H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152442194:152442194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781769990 |
| CDS Mutation | c.3889G>A |
| AA Mutation | p.Ala1297Thr(p.A1297T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367255 |
| Start | 152428359:152428359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138617999 |
| CDS Mutation | c.4822G>A |
| AA Mutation | p.Ala1608Thr(p.A1608T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152330339:152330339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14346A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152155039:152155039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746166486 |
| CDS Mutation | c.23982C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152337000:152337000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152416620:152416620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5817C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367255 |
| Start | 152442186:152442186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3897G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000367255 |
| Start | 152376497:152376497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549779256 |
| CDS Mutation | c.9208C>T |
| AA Mutation | p.Arg3070Ter(p.R3070*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367255 |
| Start | 152465257:152465257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1932+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |