Primary Site >> Stomach Cancer
Gene >> IKBKB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42316287:42316287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200322650 |
| CDS Mutation | c.878C>T |
| AA Mutation | p.Thr293Met(p.T293M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42319350:42319350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1445A>C |
| AA Mutation | p.Lys482Thr(p.K482T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42318575:42318575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781098452 |
| CDS Mutation | c.1264G>A |
| AA Mutation | p.Ala422Thr(p.A422T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42272146:42272146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.46G>A |
| AA Mutation | p.Glu16Lys(p.E16K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42322060:42322060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755267543 |
| CDS Mutation | c.1745G>A |
| AA Mutation | p.Arg582Gln(p.R582Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000520810 |
| Start | 42322090:42322090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1775G>A |
| AA Mutation | p.Arg592Gln(p.R592Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000520810 |
| Start | 42305194:42305194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201246197 |
| CDS Mutation | c.396G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000520810 |
| Start | 42320782:42320782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1626C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000520810 |
| Start | 42308984:42308984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.651G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000520810 |
| Start | 42320740:42320740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202131707 |
| CDS Mutation | c.1584C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000520810 |
| Start | 42320839:42320839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148836092 |
| CDS Mutation | c.1683C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |