Primary Site >> Stomach Cancer
Gene >> HSPA1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811528:31811528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445C>T |
| AA Mutation | p.Pro149Ser(p.P149S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811278:31811278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.695G>T |
| AA Mutation | p.Gly232Val(p.G232V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811935:31811935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.38T>C |
| AA Mutation | p.Leu13Pro(p.L13P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811899:31811899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762027845 |
| CDS Mutation | c.74A>G |
| AA Mutation | p.His25Arg(p.H25R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810794:31810794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1179G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810536:31810536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs532485515 |
| CDS Mutation | c.1437G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811355:31811355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810416:31810416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1557C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811919:31811919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.54C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811715:31811715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.258A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811280:31811280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.693T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810107:31810107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1866C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811781:31811781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.192T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811778:31811778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779903526 |
| CDS Mutation | c.195C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810845:31810845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199534532 |
| CDS Mutation | c.1128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375654 |
| Start | 31811850:31811850(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.123delC |
| AA Mutation | p.Ser42AlafsTer20(p.S42Afs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375654 |
| Start | 31810725:31810776(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1197_1248delTCCCCTGTCCCTGGGGCTGGAGACGGCTGGGGGCGTGATGACTGCCCTGATA |
| AA Mutation | p.Pro400SerfsTer25(p.P400Sfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |