Primary Site >> Stomach Cancer
Gene >> ADAMDEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256412 |
| Start | 24399452:24399452(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.989C>A |
| AA Mutation | p.Pro330Gln(p.P330Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256412 |
| Start | 24400234:24400234(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1076G>C |
| AA Mutation | p.Gly359Ala(p.G359A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256412 |
| Start | 24392373:24392373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.200G>A |
| AA Mutation | p.Gly67Asp(p.G67D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256412 |
| Start | 24400233:24400233(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1076delG |
| AA Mutation | p.Gly359ValfsTer17(p.G359Vfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256412 |
| Start | 24400173:24400173(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781693183 |
| CDS Mutation | c.1022delA |
| AA Mutation | p.Lys341ArgfsTer7(p.K341Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256412 |
| Start | 24392315:24392315(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.147delA |
| AA Mutation | p.Lys49AsnfsTer32(p.K49Nfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000256412 |
| Start | 24397427:24397427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376286647 |
| CDS Mutation | c.598C>T |
| AA Mutation | p.Arg200Ter(p.R200*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |