Primary Site >> Stomach Cancer
Gene >> LY75
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159810612:159810612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749646788 |
| CDS Mutation | c.4613G>A |
| AA Mutation | p.Arg1538Gln(p.R1538Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159852265:159852265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2819A>C |
| AA Mutation | p.Lys940Thr(p.K940T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159879337:159879337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1437G>T |
| AA Mutation | p.Glu479Asp(p.E479D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159898930:159898930(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.224T>C |
| AA Mutation | p.Leu75Pro(p.L75P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159893977:159893977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Pro192Ser(p.P192S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159894009:159894009(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.542A>G |
| AA Mutation | p.His181Arg(p.H181R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159819752:159819752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4127G>T |
| AA Mutation | p.Ser1376Ile(p.S1376I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159878383:159878383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1715C>T |
| AA Mutation | p.Ala572Val(p.A572V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159840937:159840937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559764685 |
| CDS Mutation | c.3299C>T |
| AA Mutation | p.Thr1100Met(p.T1100M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263636 |
| Start | 159840746:159840746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375167764 |
| CDS Mutation | c.3490G>A |
| AA Mutation | p.Gly1164Arg(p.G1164R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263636 |
| Start | 159875465:159875465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200795636 |
| CDS Mutation | c.1953C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |