Primary Site >> Stomach Cancer
Gene >> HSPA8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123059728:123059728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Glu289Lys(p.E289K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123058793:123058793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1361A>G |
| AA Mutation | p.Asn454Ser(p.N454S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123057754:123057754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1921A>T |
| AA Mutation | p.Thr641Ser(p.T641S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123061219:123061219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106C>G |
| AA Mutation | p.Arg36Gly(p.R36G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123060762:123060762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242C>G |
| AA Mutation | p.Ala81Gly(p.A81G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000227378 |
| Start | 123058660:123058660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1494G>C |
| AA Mutation | p.Glu498Asp(p.E498D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000227378 |
| Start | 123057902:123057902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761588256 |
| CDS Mutation | c.1773A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000227378 |
| Start | 123060736:123060738(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.266_268delATT |
| AA Mutation | p.His89_Trp90delinsArg(p.H89_W90delinsR) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |