Primary Site >> Stomach Cancer
Gene >> CLDN6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015781:3015781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374481726 |
| CDS Mutation | c.241C>T |
| AA Mutation | p.Arg81Cys(p.R81C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015717:3015717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305C>T |
| AA Mutation | p.Ala102Val(p.A102V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015371:3015371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.651G>T |
| AA Mutation | p.Lys217Asn(p.K217N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015689:3015689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.333G>T |
| AA Mutation | p.Lys111Asn(p.K111N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015511:3015511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.511T>C |
| AA Mutation | p.Ser171Pro(p.S171P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015602:3015602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771125471 |
| CDS Mutation | c.420G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015571:3015571(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.451delC |
| AA Mutation | p.Leu151TrpfsTer109(p.L151Wfs*109) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015455:3015455(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.567delG |
| AA Mutation | p.Ser190ProfsTer70(p.S190Pfs*70) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000328796 |
| Start | 3015454:3015455(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs756736939 |
| CDS Mutation | c.567dupG |
| AA Mutation | p.Ser190ValfsTer24(p.S190Vfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |