Primary Site >> Pancreatic Cancer
Gene >> CELSR3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48639957:48639957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767576418 |
| CDS Mutation | c.9628C>T |
| AA Mutation | p.Arg3210Trp(p.R3210W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48643022:48643022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8351C>T |
| AA Mutation | p.Pro2784Leu(p.P2784L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48640181:48640181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9404C>A |
| AA Mutation | p.Ala3135Asp(p.A3135D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48641998:48641998(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777442730 |
| CDS Mutation | c.8677G>A |
| AA Mutation | p.Asp2893Asn(p.D2893N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48645038:48645038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7969C>A |
| AA Mutation | p.Leu2657Met(p.L2657M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48659162:48659162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61729234 |
| CDS Mutation | c.3473G>A |
| AA Mutation | p.Arg1158His(p.R1158H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48660606:48660606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2029G>A |
| AA Mutation | p.Asp677Asn(p.D677N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48661950:48661950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.685G>T |
| AA Mutation | p.Ala229Ser(p.A229S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000164024 |
| Start | 48640236:48640236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9349C>T |
| AA Mutation | p.Arg3117Trp(p.R3117W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000164024 |
| Start | 48661270:48661270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771072162 |
| CDS Mutation | c.1365G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |