Primary Site >> Stomach Cancer
Gene >> KRT82
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52400046:52400046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199503440 |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Ala294Val(p.A294V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52406043:52406043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764314871 |
| CDS Mutation | c.235G>A |
| AA Mutation | p.Gly79Arg(p.G79R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52395084:52395084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433G>T |
| AA Mutation | p.Gly478Val(p.G478V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52394982:52394982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1535A>C |
| AA Mutation | p.Lys512Thr(p.K512T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52400011:52400011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376327776 |
| CDS Mutation | c.916G>A |
| AA Mutation | p.Glu306Lys(p.E306K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52406267:52406267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11A>T |
| AA Mutation | p.His4Leu(p.H4L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257974 |
| Start | 52396054:52396054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1247A>T |
| AA Mutation | p.Glu416Val(p.E416V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257974 |
| Start | 52406202:52406202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.76C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257974 |
| Start | 52405885:52405885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149898957 |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257974 |
| Start | 52395065:52395065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs544286686 |
| CDS Mutation | c.1452C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257974 |
| Start | 52400578:52400578(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370016325 |
| CDS Mutation | c.726C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257974 |
| Start | 52395151:52395151(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1366delG |
| AA Mutation | p.Val456SerfsTer35(p.V456Sfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |