Primary Site >> Pancreatic Cancer
Gene >> MAP1B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199044:72199044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757286026 |
| CDS Mutation | c.5689C>T |
| AA Mutation | p.Arg1897Trp(p.R1897W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199257:72199257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5902G>A |
| AA Mutation | p.Glu1968Lys(p.E1968K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72196023:72196023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139604402 |
| CDS Mutation | c.2668G>A |
| AA Mutation | p.Glu890Lys(p.E890K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72197080:72197080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3725G>A |
| AA Mutation | p.Ser1242Asn(p.S1242N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199249:72199249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5894G>T |
| AA Mutation | p.Ser1965Ile(p.S1965I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199514:72199514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6159G>T |
| AA Mutation | p.Gln2053His(p.Q2053H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296755 |
| Start | 72199993:72199993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754794035 |
| CDS Mutation | c.6638G>A |
| AA Mutation | p.Arg2213His(p.R2213H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296755 |
| Start | 72194345:72194345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.990G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000296755 |
| Start | 72194714:72194714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1359G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000296755 |
| Start | 72194262:72194262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.907C>T |
| AA Mutation | p.Arg303Ter(p.R303*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |