Primary Site >> Stomach Cancer
Gene >> CR1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367051 |
| Start | 207511653:207511653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.486C>G |
| AA Mutation | p.Asp162Glu(p.D162E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207577916:207577916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769092015 |
| CDS Mutation | c.3299G>C |
| AA Mutation | p.Arg1100Thr(p.R1100T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207577963:207577963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3346A>G |
| AA Mutation | p.Thr1116Ala(p.T1116A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207584750:207584750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4054C>T |
| AA Mutation | p.Pro1352Ser(p.P1352S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000367051 |
| Start | 207575596:207575596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3103C>T |
| AA Mutation | p.His1035Tyr(p.H1035Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207565867:207565867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2546A>G |
| AA Mutation | p.Tyr849Cys(p.Y849C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207577996:207577996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749316044 |
| CDS Mutation | c.3379G>A |
| AA Mutation | p.Gly1127Ser(p.G1127S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207505936:207505936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154G>T |
| AA Mutation | p.Ala52Ser(p.A52S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207580549:207580549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3802G>T |
| AA Mutation | p.Gly1268Cys(p.G1268C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207580363:207580363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3710C>T |
| AA Mutation | p.Ser1237Phe(p.S1237F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207505927:207505927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145C>T |
| AA Mutation | p.Leu49Phe(p.L49F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207611686:207611686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs561028518 |
| CDS Mutation | c.4955C>T |
| AA Mutation | p.Pro1652Leu(p.P1652L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207578002:207578002(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201139679 |
| CDS Mutation | c.3385G>A |
| AA Mutation | p.Ala1129Thr(p.A1129T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207607262:207607262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4472T>G |
| AA Mutation | p.Ile1491Ser(p.I1491S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207565917:207565917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2596T>C |
| AA Mutation | p.Cys866Arg(p.C866R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207563959:207563959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2332C>T |
| AA Mutation | p.Pro778Ser(p.P778S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207580399:207580399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3746A>C |
| AA Mutation | p.Glu1249Ala(p.E1249A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207616616:207616616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5353C>T |
| AA Mutation | p.His1785Tyr(p.H1785Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207618093:207618093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772261193 |
| CDS Mutation | c.5562C>G |
| AA Mutation | p.Ile1854Met(p.I1854M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207505999:207505999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.217T>C |
| AA Mutation | p.Cys73Arg(p.C73R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367051 |
| Start | 207506003:207506003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200913967 |
| CDS Mutation | c.221G>A |
| AA Mutation | p.Arg74His(p.R74H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207618120:207618120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765243201 |
| CDS Mutation | c.5589C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207564027:207564027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2400C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207496312:207496312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375945701 |
| CDS Mutation | c.45G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207578073:207578073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207545429:207545429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556651959 |
| CDS Mutation | c.1008G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367051 |
| Start | 207563985:207563985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2358G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000367051 |
| Start | 207506084:207506084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199647026 |
| CDS Mutation | c.301+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |