Primary Site >> Stomach Cancer
Gene >> SIGLEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3691450:3691450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4481C>A |
| AA Mutation | p.Pro1494His(p.P1494H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694771:3694771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2836C>T |
| AA Mutation | p.Arg946Cys(p.R946C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3691462:3691462(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147117268 |
| CDS Mutation | c.4469C>T |
| AA Mutation | p.Ala1490Val(p.A1490V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3688576:3688576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5114C>T |
| AA Mutation | p.Ala1705Val(p.A1705V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3689204:3689204(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5021G>A |
| AA Mutation | p.Ser1674Asn(p.S1674N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3706506:3706506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140311277 |
| CDS Mutation | c.250C>T |
| AA Mutation | p.Arg84Cys(p.R84C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| 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 | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693554:3693554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3401T>C |
| AA Mutation | p.Ile1134Thr(p.I1134T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3691420:3691420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4511C>T |
| AA Mutation | p.Ala1504Val(p.A1504V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3699255:3699255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1733G>A |
| AA Mutation | p.Arg578Gln(p.R578Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3703299:3703299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754492228 |
| CDS Mutation | c.1126C>T |
| AA Mutation | p.Arg376Trp(p.R376W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3698085:3698085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835C>A |
| AA Mutation | p.Ala612Asp(p.A612D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3705867:3705867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111336308 |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Gly195Ser(p.G195S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3689178:3689178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5047G>A |
| AA Mutation | p.Ala1683Thr(p.A1683T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3690172:3690172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773583320 |
| CDS Mutation | c.4684G>A |
| AA Mutation | p.Ala1562Thr(p.A1562T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694469:3694469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3008T>A |
| AA Mutation | p.Leu1003His(p.L1003H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694523:3694523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2954G>A |
| AA Mutation | p.Arg985His(p.R985H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3697816:3697816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2104G>T |
| AA Mutation | p.Ala702Ser(p.A702S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3697955:3697955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1965C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3691464:3691464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772977310 |
| CDS Mutation | c.4467C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3703294:3703294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1131G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3692003:3692003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4230G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3696746:3696746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2523T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3692591:3692591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376077734 |
| CDS Mutation | c.3960C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693085:3693085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144602570 |
| CDS Mutation | c.3555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3696725:3696725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2544T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3706009:3706009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772977227 |
| CDS Mutation | c.441G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3698129:3698129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1791C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3703270:3703270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693016:3693016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3624C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344754 |
| Start | 3698027:3698027(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757222868 |
| CDS Mutation | c.1893delC |
| AA Mutation | p.Ala632ProfsTer32(p.A632Pfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344754 |
| Start | 3703844:3703844(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.954delC |
| AA Mutation | p.Ile319SerfsTer12(p.I319Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000344754 |
| Start | 3694482:3694482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556514664 |
| CDS Mutation | c.2995C>T |
| AA Mutation | p.Arg999Ter(p.R999*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |