Primary Site >> Stomach Cancer
Gene >> CLIP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29160385:29160385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1452A>T |
| AA Mutation | p.Glu484Asp(p.E484D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181592:29181592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760697191 |
| CDS Mutation | c.1817G>A |
| AA Mutation | p.Arg606His(p.R606H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181841:29181841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2066G>T |
| AA Mutation | p.Arg689Ile(p.R689I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29143781:29143781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201519559 |
| CDS Mutation | c.721G>A |
| AA Mutation | p.Ala241Thr(p.A241T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181687:29181687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1912G>T |
| AA Mutation | p.Gly638Cys(p.G638C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181594:29181594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200138252 |
| CDS Mutation | c.1819A>G |
| AA Mutation | p.Ser607Gly(p.S607G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181835:29181835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373598789 |
| CDS Mutation | c.2060C>T |
| AA Mutation | p.Pro687Leu(p.P687L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320081 |
| Start | 29135623:29135623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.605C>T |
| AA Mutation | p.Ala202Val(p.A202V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181758:29181758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1983C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181647:29181647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1872C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181815:29181815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2040C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29133806:29133806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150045383 |
| CDS Mutation | c.519G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29163892:29163892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1596T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320081 |
| Start | 29181707:29181707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755004717 |
| CDS Mutation | c.1932C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |