Primary Site >> Stomach Cancer
Gene >> BAIAP2L1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98304306:98304306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1312G>A |
| AA Mutation | p.Asp438Asn(p.D438N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98317248:98317248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151171453 |
| CDS Mutation | c.457G>A |
| AA Mutation | p.Ala153Thr(p.A153T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98317314:98317314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.391G>A |
| AA Mutation | p.Glu131Lys(p.E131K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98306490:98306490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768990780 |
| CDS Mutation | c.1190C>T |
| AA Mutation | p.Thr397Met(p.T397M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98304353:98304353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs76206450 |
| CDS Mutation | c.1265G>A |
| AA Mutation | p.Ser422Asn(p.S422N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000005260 |
| Start | 98362401:98362401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368033137 |
| CDS Mutation | c.83G>A |
| AA Mutation | p.Arg28Gln(p.R28Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005260 |
| Start | 98355120:98355120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.136C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000005260 |
| Start | 98317249:98317249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764805259 |
| CDS Mutation | c.456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |