Primary Site >> Pancreatic Cancer
Gene >> SIGLEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693039:3693039(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753045959 |
| CDS Mutation | c.3601G>A |
| AA Mutation | p.Ala1201Thr(p.A1201T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3701480:3701480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200340665 |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Arg464Cys(p.R464C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693555:3693555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779166120 |
| CDS Mutation | c.3400A>G |
| AA Mutation | p.Ile1134Val(p.I1134V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3689219:3689219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763965082 |
| CDS Mutation | c.5006G>A |
| AA Mutation | p.Arg1669His(p.R1669H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3692595:3692595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762704738 |
| CDS Mutation | c.3956C>T |
| AA Mutation | p.Ala1319Val(p.A1319V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3692751:3692751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150431597 |
| CDS Mutation | c.3800C>T |
| AA Mutation | p.Pro1267Leu(p.P1267L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693023:3693023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3617G>T |
| AA Mutation | p.Ser1206Ile(p.S1206I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3699310:3699310(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1678C>A |
| AA Mutation | p.Leu560Ile(p.L560I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3701479:3701479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34924243 |
| CDS Mutation | c.1391G>A |
| AA Mutation | p.Arg464His(p.R464H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3698036:3698036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1884C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |