Primary Site >> Stomach Cancer
Gene >> HLA-C
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376228 |
| Start | 31271223:31271223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.469T>C |
| AA Mutation | p.Trp157Arg(p.W157R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376228 |
| Start | 31271141:31271141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.551T>C |
| AA Mutation | p.Leu184Pro(p.L184P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376228 |
| Start | 31272040:31272040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.32T>C |
| AA Mutation | p.Leu11Pro(p.L11P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376228 |
| Start | 31271695:31271695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.247T>C |
| AA Mutation | p.Tyr83His(p.Y83H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000376228 |
| Start | 31269173:31269173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097C>G |
| AA Mutation | p.Ala366Gly(p.A366G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376228 |
| Start | 31269497:31269497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1044T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000376228 |
| Start | 31271691:31271691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs281860390 |
| CDS Mutation | c.251G>A |
| AA Mutation | p.Trp84Ter(p.W84*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000376228 |
| Start | 31271139:31271139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.553G>T |
| AA Mutation | p.Glu185Ter(p.E185*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000376228 |
| Start | 31271205:31271206(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.482_486dupACACC |
| AA Mutation | p.Ala163ThrfsTer20(p.A163Tfs*20) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000376228 |
| Start | 31271334:31271336(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.356_358delTCC |
| AA Mutation | p.Leu119del(p.L119del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |