Primary Site >> Stomach Cancer
Gene >> ADAM23
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206565032:206565032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1358C>A |
| AA Mutation | p.Thr453Lys(p.T453K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206596126:206596126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2323A>G |
| AA Mutation | p.Arg775Gly(p.R775G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206560089:206560089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1140G>T |
| AA Mutation | p.Lys380Asn(p.K380N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206570773:206570773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540276873 |
| CDS Mutation | c.1528G>A |
| AA Mutation | p.Val510Met(p.V510M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206571784:206571784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377327401 |
| CDS Mutation | c.1624G>A |
| AA Mutation | p.Asp542Asn(p.D542N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206594790:206594790(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2132G>T |
| AA Mutation | p.Gly711Val(p.G711V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264377 |
| Start | 206562203:206562203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1255T>C |
| AA Mutation | p.Tyr419His(p.Y419H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264377 |
| Start | 206548344:206548344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857G>T |
| AA Mutation | p.Arg286Ile(p.R286I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264377 |
| Start | 206594806:206594806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750323915 |
| CDS Mutation | c.2148G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264377 |
| Start | 206548330:206548330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264377 |
| Start | 206594794:206594794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540645451 |
| CDS Mutation | c.2136G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264377 |
| Start | 206542090:206542090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780126514 |
| CDS Mutation | c.612C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |