Primary Site >> Pancreatic Cancer
Gene >> FLT4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180612570:180612570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3473C>T |
| AA Mutation | p.Ala1158Val(p.A1158V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180611401:180611401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3616G>A |
| AA Mutation | p.Ala1206Thr(p.A1206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180619743:180619743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267606818 |
| CDS Mutation | c.2569G>A |
| AA Mutation | p.Gly857Arg(p.G857R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180629812:180629812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.700C>A |
| AA Mutation | p.Leu234Met(p.L234M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180630602:180630602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.353C>T |
| AA Mutation | p.Ala118Val(p.A118V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261937 |
| Start | 180624060:180624060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768956955 |
| CDS Mutation | c.1423C>T |
| AA Mutation | p.Arg475Trp(p.R475W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261937 |
| Start | 180612610:180612610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202140363 |
| CDS Mutation | c.3433C>T |
| AA Mutation | p.Arg1145Cys(p.R1145C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261937 |
| Start | 180630054:180630054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.565C>T |
| AA Mutation | p.Arg189Trp(p.R189W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261937 |
| Start | 180621549:180621549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2013G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261937 |
| Start | 180628887:180628887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000261937 |
| Start | 180629837:180629837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.677-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |