Primary Site >> Stomach Cancer
Gene >> SMARCB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23787232:23787232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.63C>A |
| AA Mutation | p.Asp21Glu(p.D21E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23834152:23834152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs387906812 |
| CDS Mutation | c.1130G>A |
| AA Mutation | p.Arg377His(p.R377H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23801045:23801045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.464G>A |
| AA Mutation | p.Arg155His(p.R155H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23825363:23825363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749348930 |
| CDS Mutation | c.934G>A |
| AA Mutation | p.Ala312Thr(p.A312T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23825348:23825348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.919T>G |
| AA Mutation | p.Phe307Val(p.F307V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23793564:23793564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754395342 |
| CDS Mutation | c.238G>A |
| AA Mutation | p.Gly80Arg(p.G80R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263121 |
| Start | 23791781:23791781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.119G>A |
| AA Mutation | p.Arg40Gln(p.R40Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263121 |
| Start | 23803331:23803331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533184210 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263121 |
| Start | 23793563:23793563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200394488 |
| CDS Mutation | c.237C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |