Primary Site >> Pancreatic Cancer
Gene >> DAAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59353947:59353947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2369T>C |
| AA Mutation | p.Val790Ala(p.V790A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59330595:59330595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1467A>C |
| AA Mutation | p.Lys489Asn(p.K489N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59347567:59347567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749346775 |
| CDS Mutation | c.2134C>T |
| AA Mutation | p.Arg712Trp(p.R712W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59368744:59368744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3122G>T |
| AA Mutation | p.Arg1041Leu(p.R1041L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000395125 |
| Start | 59322933:59322933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.482T>G |
| AA Mutation | p.Ile161Ser(p.I161S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000395125 |
| Start | 59263558:59263558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776785504 |
| CDS Mutation | c.81G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000395125 |
| Start | 59326976:59326977(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1363dupA |
| AA Mutation | p.Met455AsnfsTer7(p.M455Nfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |