Primary Site >> Stomach Cancer
Gene >> LZTR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20985888:20985888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.311C>G |
| AA Mutation | p.Ser104Cys(p.S104C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20982554:20982554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.183C>A |
| AA Mutation | p.Asp61Glu(p.D61E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20996739:20996739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141161152 |
| CDS Mutation | c.2263C>T |
| AA Mutation | p.Arg755Trp(p.R755W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20992878:20992878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747430075 |
| CDS Mutation | c.1234C>T |
| AA Mutation | p.Arg412Cys(p.R412C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20988097:20988097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200806641 |
| CDS Mutation | c.488C>T |
| AA Mutation | p.Thr163Met(p.T163M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20993720:20993720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764415634 |
| CDS Mutation | c.1319G>A |
| AA Mutation | p.Arg440His(p.R440H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20994996:20994996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1912C>T |
| AA Mutation | p.Arg638Cys(p.R638C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20996928:20996928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767637944 |
| CDS Mutation | c.2368C>T |
| AA Mutation | p.Arg790Trp(p.R790W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20985867:20985867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.290G>A |
| AA Mutation | p.Arg97Gln(p.R97Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20990476:20990476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.742G>A |
| AA Mutation | p.Gly248Arg(p.G248R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20995794:20995794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776112712 |
| CDS Mutation | c.1991C>T |
| AA Mutation | p.Ala664Val(p.A664V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20991677:20991677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.841C>A |
| AA Mutation | p.Pro281Thr(p.P281T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20994647:20994647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1705T>C |
| AA Mutation | p.Tyr569His(p.Y569H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20996062:20996062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2169G>A |
| AA Mutation | p.Met723Ile(p.M723I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215739 |
| Start | 20992854:20992854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1210G>A |
| AA Mutation | p.Gly404Arg(p.G404R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215739 |
| Start | 20993751:20993751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1350T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215739 |
| Start | 20992252:20992252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375479373 |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |