Primary Site >> Stomach Cancer
Gene >> CNTRL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121173381:121173381(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6556C>G |
| AA Mutation | p.Leu2186Val(p.L2186V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121150255:121150255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3735G>T |
| AA Mutation | p.Met1245Ile(p.M1245I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121164976:121164976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5457G>T |
| AA Mutation | p.Met1819Ile(p.M1819I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121157771:121157771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4528C>G |
| AA Mutation | p.Gln1510Glu(p.Q1510E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121135911:121135911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769763623 |
| CDS Mutation | c.2131C>T |
| AA Mutation | p.Arg711Trp(p.R711W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121158045:121158045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4700T>A |
| AA Mutation | p.Val1567Asp(p.V1567D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121141409:121141409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2512A>G |
| AA Mutation | p.Lys838Glu(p.K838E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121173721:121173721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764424296 |
| CDS Mutation | c.6731G>A |
| AA Mutation | p.Arg2244Gln(p.R2244Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121135858:121135858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2078C>T |
| AA Mutation | p.Ser693Phe(p.S693F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000238341 |
| Start | 121096520:121096520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.578A>C |
| AA Mutation | p.Lys193Thr(p.K193T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238341 |
| Start | 121145348:121145348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3273T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238341 |
| Start | 121138667:121138667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2325T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000238341 |
| Start | 121162201:121162201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5353T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238341 |
| Start | 121162247:121162247(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5405delA |
| AA Mutation | p.Lys1802SerfsTer9(p.K1802Sfs*9) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000238341 |
| Start | 121150412:121150412(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3897delC |
| AA Mutation | p.Asn1300ThrfsTer22(p.N1300Tfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000238341 |
| Start | 121166112:121166112(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199993226 |
| CDS Mutation | c.5587C>T |
| AA Mutation | p.Arg1863Ter(p.R1863*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |