Primary Site >> Stomach Cancer
Gene >> GABRQ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152651745:152651745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374His(p.R374H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152651702:152651702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1078C>T |
| AA Mutation | p.Arg360Cys(p.R360C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152651570:152651570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376489228 |
| CDS Mutation | c.946C>T |
| AA Mutation | p.Arg316Trp(p.R316W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652851:152652851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469G>T |
| AA Mutation | p.Gly490Val(p.G490V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000598523 |
| Start | 152640464:152640464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.236G>T |
| AA Mutation | p.Gly79Val(p.G79V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152638261:152638261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.59T>G |
| AA Mutation | p.Leu20Arg(p.L20R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152647122:152647122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782042263 |
| CDS Mutation | c.481C>T |
| AA Mutation | p.Arg161Cys(p.R161C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652705:152652705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1323G>T |
| AA Mutation | p.Gln441His(p.Q441H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152638276:152638276(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.74A>G |
| AA Mutation | p.Tyr25Cys(p.Y25C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152651730:152651730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782675594 |
| CDS Mutation | c.1106G>A |
| AA Mutation | p.Arg369Gln(p.R369Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652622:152652622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374632460 |
| CDS Mutation | c.1240C>T |
| AA Mutation | p.Leu414Phe(p.L414F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652951:152652951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1569C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652753:152652753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1371A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652813:152652813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1431T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152650468:152650468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782570875 |
| CDS Mutation | c.789G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152649257:152649257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.534C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000598523 |
| Start | 152652735:152652735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372512790 |
| CDS Mutation | c.1353C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |