Primary Site >> Stomach Cancer
Gene >> PTGS1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122378504:122378504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753672636 |
| CDS Mutation | c.283G>A |
| AA Mutation | p.Gly95Arg(p.G95R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122392321:122392321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1577C>T |
| AA Mutation | p.Ala526Val(p.A526V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122392489:122392489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201836968 |
| CDS Mutation | c.1745C>T |
| AA Mutation | p.Pro582Leu(p.P582L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122377961:122377961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Cys(p.R53C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000362012 |
| Start | 122378015:122378015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143357990 |
| CDS Mutation | c.211C>T |
| AA Mutation | p.Pro71Ser(p.P71S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122381448:122381448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.574G>T |
| AA Mutation | p.Gly192Cys(p.G192C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122381673:122381673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs3842795 |
| CDS Mutation | c.688G>A |
| AA Mutation | p.Gly230Ser(p.G230S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122392515:122392515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1771G>A |
| AA Mutation | p.Ala591Thr(p.A591T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122377946:122377946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368356508 |
| CDS Mutation | c.142C>T |
| AA Mutation | p.Arg48Cys(p.R48C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122392366:122392366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753219685 |
| CDS Mutation | c.1622C>T |
| AA Mutation | p.Pro541Leu(p.P541L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122378787:122378787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.365T>G |
| AA Mutation | p.Leu122Arg(p.L122R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122392482:122392482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1738C>T |
| AA Mutation | p.Arg580Cys(p.R580C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122378858:122378858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436T>C |
| AA Mutation | p.Tyr146His(p.Y146H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000362012 |
| Start | 122381700:122381700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Cys(p.R239C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362012 |
| Start | 122383583:122383583(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760743281 |
| CDS Mutation | c.837G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000362012 |
| Start | 122377951:122377951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138230380 |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000362012 |
| Start | 122378798:122378798(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779702921 |
| CDS Mutation | c.381delC |
| AA Mutation | p.Thr128ProfsTer17(p.T128Pfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |