Primary Site >> Pancreatic Cancer
Gene >> CNTN4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397461 |
| Start | 3037212:3037212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151038163 |
| CDS Mutation | c.1976C>T |
| AA Mutation | p.Ala659Val(p.A659V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397461 |
| Start | 2819564:2819564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.437C>T |
| AA Mutation | p.Pro146Leu(p.P146L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397461 |
| Start | 2866803:2866803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761504879 |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169His(p.R169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397461 |
| Start | 2887090:2887090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.806G>T |
| AA Mutation | p.Arg269Met(p.R269M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397461 |
| Start | 3026156:3026156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Ser514Asn(p.S514N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000397461 |
| Start | 3043164:3043164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2698+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |