Primary Site >> Stomach Cancer
Gene >> ERCC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45364085:45364085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.850G>A |
| AA Mutation | p.Glu284Lys(p.E284K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45352757:45352757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144511865 |
| CDS Mutation | c.1891C>T |
| AA Mutation | p.Arg631Cys(p.R631C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45355677:45355677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1531C>T |
| AA Mutation | p.Arg511Trp(p.R511W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45364918:45364918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs559154781 |
| CDS Mutation | c.514G>A |
| AA Mutation | p.Ala172Thr(p.A172T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45365052:45365052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201294521 |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Arg156Gln(p.R156Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45361617:45361617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1144C>A |
| AA Mutation | p.Leu382Met(p.L382M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45357533:45357533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768677952 |
| CDS Mutation | c.1318G>A |
| AA Mutation | p.Ala440Thr(p.A440T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45364057:45364057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Arg293Gln(p.R293Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45364326:45364326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.724G>A |
| AA Mutation | p.Val242Ile(p.V242I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45353262:45353262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751318902 |
| CDS Mutation | c.1738G>A |
| AA Mutation | p.Ala580Thr(p.A580T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391945 |
| Start | 45364091:45364091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375415853 |
| CDS Mutation | c.844C>T |
| AA Mutation | p.Arg282Trp(p.R282W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391945 |
| Start | 45352782:45352782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs16979773 |
| CDS Mutation | c.1866C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000391945 |
| Start | 45352628:45352628(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1924delG |
| AA Mutation | p.Asp642ThrfsTer67(p.D642Tfs*67) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |