Primary Site >> Stomach Cancer
Gene >> BCL7C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215115 |
| Start | 30892603:30892603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142Gln(p.R142Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000215115 |
| Start | 30887990:30887990(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.529G>T |
| AA Mutation | p.Ala177Ser(p.A177S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215115 |
| Start | 30892912:30892912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188345023 |
| CDS Mutation | c.208C>T |
| AA Mutation | p.Arg70Cys(p.R70C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215115 |
| Start | 30893238:30893238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145G>A |
| AA Mutation | p.Val49Met(p.V49M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215115 |
| Start | 30892929:30892929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Gly64Asp(p.G64D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000215115 |
| Start | 30887984:30887984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760033767 |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Glu179Lys(p.E179K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000215115 |
| Start | 30892644:30892644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145075832 |
| CDS Mutation | c.384C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000215115 |
| Start | 30892670:30892670(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758526156 |
| CDS Mutation | c.358delC |
| AA Mutation | p.Gln120SerfsTer33(p.Q120Sfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000215115 |
| Start | 30887901:30887902(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs767347334 |
| CDS Mutation | c.617dupC |
| AA Mutation | p.Leu207ThrfsTer10(p.L207Tfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |