Primary Site >> Stomach Cancer
Gene >> TLN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35719100:35719100(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373629805 |
| CDS Mutation | c.1870C>T |
| AA Mutation | p.Arg624Cys(p.R624C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35722159:35722159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773595542 |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Arg303His(p.R303H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35724277:35724277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769874189 |
| CDS Mutation | c.569C>T |
| AA Mutation | p.Thr190Met(p.T190M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35704047:35704047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757869013 |
| CDS Mutation | c.6175G>A |
| AA Mutation | p.Ala2059Thr(p.A2059T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35713201:35713201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3347A>T |
| AA Mutation | p.Tyr1116Phe(p.Y1116F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35713996:35713996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3206C>T |
| AA Mutation | p.Ala1069Val(p.A1069V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35714792:35714792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570598486 |
| CDS Mutation | c.2839G>A |
| AA Mutation | p.Gly947Ser(p.G947S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35705805:35705805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5558A>G |
| AA Mutation | p.Tyr1853Cys(p.Y1853C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000314888 |
| Start | 35720040:35720040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1463T>C |
| AA Mutation | p.Leu488Pro(p.L488P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35704435:35704435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5944G>A |
| AA Mutation | p.Ala1982Thr(p.A1982T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35711735:35711735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3739G>A |
| AA Mutation | p.Ala1247Thr(p.A1247T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35717229:35717229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2375C>T |
| AA Mutation | p.Ala792Val(p.A792V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35711381:35711381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189605894 |
| CDS Mutation | c.3893G>A |
| AA Mutation | p.Arg1298Gln(p.R1298Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35711656:35711656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747462166 |
| CDS Mutation | c.3818G>A |
| AA Mutation | p.Arg1273Gln(p.R1273Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35725616:35725616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.79G>A |
| AA Mutation | p.Asp27Asn(p.D27N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35714860:35714860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2771C>T |
| AA Mutation | p.Ala924Val(p.A924V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35716446:35716446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2569T>G |
| AA Mutation | p.Leu857Val(p.L857V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35706865:35706865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766069516 |
| CDS Mutation | c.4991C>T |
| AA Mutation | p.Ala1664Val(p.A1664V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35697861:35697861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7556G>A |
| AA Mutation | p.Arg2519Gln(p.R2519Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35715066:35715066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760405428 |
| CDS Mutation | c.2747G>A |
| AA Mutation | p.Arg916His(p.R916H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35707796:35707796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4567C>T |
| AA Mutation | p.Arg1523Cys(p.R1523C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35719205:35719205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759490877 |
| CDS Mutation | c.1765C>T |
| AA Mutation | p.Arg589Cys(p.R589C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35719123:35719123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756483237 |
| CDS Mutation | c.1847C>T |
| AA Mutation | p.Ala616Val(p.A616V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35717292:35717292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2312C>T |
| AA Mutation | p.Ala771Val(p.A771V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35706105:35706105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754790750 |
| CDS Mutation | c.5368G>A |
| AA Mutation | p.Ala1790Thr(p.A1790T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35707153:35707153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4874G>A |
| AA Mutation | p.Arg1625Gln(p.R1625Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000314888 |
| Start | 35708387:35708387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4424A>G |
| AA Mutation | p.Gln1475Arg(p.Q1475R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314888 |
| Start | 35713242:35713242(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778146857 |
| CDS Mutation | c.3306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314888 |
| Start | 35721735:35721735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1017A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000314888 |
| Start | 35725617:35725617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755651034 |
| CDS Mutation | c.78C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |