Primary Site >> Pancreatic Cancer
Gene >> SCN5A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38581182:38581182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770088052 |
| CDS Mutation | c.2977G>A |
| AA Mutation | p.Ala993Thr(p.A993T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38560374:38560374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473605 |
| CDS Mutation | c.4018G>A |
| AA Mutation | p.Val1340Ile(p.V1340I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38620901:38620901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192113333 |
| CDS Mutation | c.553G>A |
| AA Mutation | p.Ala185Thr(p.A185T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38597926:38597926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473580 |
| CDS Mutation | c.2065C>T |
| AA Mutation | p.Arg689Cys(p.R689C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38550577:38550577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371194826 |
| CDS Mutation | c.5795C>T |
| AA Mutation | p.Ala1932Val(p.A1932V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38562467:38562467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199473603 |
| CDS Mutation | c.3911C>T |
| AA Mutation | p.Thr1304Met(p.T1304M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000333535 |
| Start | 38575299:38575299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3664C>A |
| AA Mutation | p.Leu1222Met(p.L1222M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38581080:38581080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3079C>T |
| AA Mutation | p.Arg1027Trp(p.R1027W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38581313:38581313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2846C>T |
| AA Mutation | p.Ala949Val(p.A949V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333535 |
| Start | 38551004:38551004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772508476 |
| CDS Mutation | c.5368G>A |
| AA Mutation | p.Asp1790Asn(p.D1790N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38585931:38585931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2547C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38575357:38575357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3606G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38606053:38606053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs45565936 |
| CDS Mutation | c.1236C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333535 |
| Start | 38630340:38630340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.363G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |