Primary Site >> Stomach Cancer
Gene >> CSE1L
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49096388:49096388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769741319 |
| CDS Mutation | c.2866C>A |
| AA Mutation | p.Leu956Ile(p.L956I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49063253:49063253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.137T>C |
| AA Mutation | p.Leu46Pro(p.L46P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49072380:49072380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773313816 |
| CDS Mutation | c.863G>A |
| AA Mutation | p.Arg288Gln(p.R288Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49066225:49066225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.262G>A |
| AA Mutation | p.Asp88Asn(p.D88N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49084107:49084107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746788725 |
| CDS Mutation | c.1564G>A |
| AA Mutation | p.Ala522Thr(p.A522T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49072343:49072343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149344844 |
| CDS Mutation | c.826G>A |
| AA Mutation | p.Ala276Thr(p.A276T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49063255:49063255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.139T>A |
| AA Mutation | p.Leu47Met(p.L47M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262982 |
| Start | 49072392:49072392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746870335 |
| CDS Mutation | c.875G>A |
| AA Mutation | p.Arg292His(p.R292H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262982 |
| Start | 49072600:49072600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.969A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262982 |
| Start | 49096363:49096363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2841G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262982 |
| Start | 49085307:49085307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112036311 |
| CDS Mutation | c.1644G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262982 |
| Start | 49066254:49066254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.291G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262982 |
| Start | 49075370:49075371(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1191dupT |
| AA Mutation | p.Glu398Ter(p.E398*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |