Primary Site >> Stomach Cancer
Gene >> KNG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186739144:186739144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.976A>G |
| AA Mutation | p.Thr326Ala(p.T326A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186731591:186731591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369801278 |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240Gln(p.R240Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186727302:186727302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630T>G |
| AA Mutation | p.Asn210Lys(p.N210K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186741865:186741865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469T>C |
| AA Mutation | p.Val490Ala(p.V490A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186741742:186741742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346G>A |
| AA Mutation | p.Arg449His(p.R449H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186739150:186739150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.982T>C |
| AA Mutation | p.Cys328Arg(p.C328R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186741576:186741576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1180G>A |
| AA Mutation | p.Gly394Arg(p.G394R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265023 |
| Start | 186732537:186732537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145150298 |
| CDS Mutation | c.793G>A |
| AA Mutation | p.Val265Met(p.V265M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265023 |
| Start | 186720137:186720137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142661545 |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265023 |
| Start | 186725122:186725122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.426C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265023 |
| Start | 186727251:186727251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.579G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000265023 |
| Start | 186741914:186741915(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1523dupA |
| AA Mutation | p.Asn508LysfsTer2(p.N508Kfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |