Primary Site >> Pancreatic Cancer
Gene >> SYNE2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64052306:64052306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8393C>T |
| AA Mutation | p.Thr2798Ile(p.T2798I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64113498:64113498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs552966507 |
| CDS Mutation | c.12767A>G |
| AA Mutation | p.Asn4256Ser(p.N4256S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000344113 |
| Start | 64002081:64002081(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3786G>C |
| AA Mutation | p.Arg1262Ser(p.R1262S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 63967794:63967794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1076T>C |
| AA Mutation | p.Leu359Pro(p.L359P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64022790:64022790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5564A>G |
| AA Mutation | p.Lys1855Arg(p.K1855R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64030016:64030016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6836C>A |
| AA Mutation | p.Pro2279His(p.P2279H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64051687:64051687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7774G>A |
| AA Mutation | p.Asp2592Asn(p.D2592N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64051749:64051749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7836G>T |
| AA Mutation | p.Gln2612His(p.Q2612H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64053641:64053641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9728G>T |
| AA Mutation | p.Ser3243Ile(p.S3243I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64065550:64065550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372338837 |
| CDS Mutation | c.10331C>T |
| AA Mutation | p.Ser3444Leu(p.S3444L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64158648:64158648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15816G>A |
| AA Mutation | p.Met5272Ile(p.M5272I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64170418:64170418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376008959 |
| CDS Mutation | c.17191C>T |
| AA Mutation | p.Arg5731Cys(p.R5731C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64225369:64225369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756327978 |
| CDS Mutation | c.20501G>A |
| AA Mutation | p.Arg6834Gln(p.R6834Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344113 |
| Start | 64214356:64214356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19219G>A |
| AA Mutation | p.Glu6407Lys(p.E6407K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344113 |
| Start | 64137816:64137816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375987275 |
| CDS Mutation | c.14676C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344113 |
| Start | 64212936:64212936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18987C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344113 |
| Start | 64224526:64224526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546213944 |
| CDS Mutation | c.20379C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000344113 |
| Start | 64052401:64052401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8488G>T |
| AA Mutation | p.Glu2830Ter(p.E2830*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000344113 |
| Start | 64075944:64075944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10867-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |