Primary Site >> Stomach Cancer
Gene >> HK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69382767:69382767(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1546G>A |
| AA Mutation | p.Val516Ile(p.V516I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69398674:69398674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771865870 |
| CDS Mutation | c.2455G>A |
| AA Mutation | p.Val819Ile(p.V819I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69368627:69368627(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.587G>A |
| AA Mutation | p.Arg196Gln(p.R196Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69384399:69384399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548019222 |
| CDS Mutation | c.1637G>A |
| AA Mutation | p.Arg546His(p.R546H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69382536:69382536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1315G>A |
| AA Mutation | p.Asp439Asn(p.D439N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69364865:69364865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.458C>T |
| AA Mutation | p.Thr153Met(p.T153M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69382498:69382498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1277G>A |
| AA Mutation | p.Arg426His(p.R426H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69384371:69384371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1609A>C |
| AA Mutation | p.Asn537His(p.N537H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69382594:69382594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1373C>T |
| AA Mutation | p.Ala458Val(p.A458V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69369327:69369327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.682C>A |
| AA Mutation | p.Leu228Met(p.L228M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69392280:69392280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2191G>A |
| AA Mutation | p.Glu731Lys(p.E731K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69398777:69398777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538768945 |
| CDS Mutation | c.2558G>A |
| AA Mutation | p.Arg853His(p.R853H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69382758:69382758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1537C>T |
| AA Mutation | p.Pro513Ser(p.P513S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69395054:69395054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2324C>T |
| AA Mutation | p.Thr775Met(p.T775M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69369552:69369552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.803G>A |
| AA Mutation | p.Gly268Glu(p.G268E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69379903:69379903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747980178 |
| CDS Mutation | c.1073G>A |
| AA Mutation | p.Arg358His(p.R358H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69368575:69368575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.535G>A |
| AA Mutation | p.Gly179Arg(p.G179R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69368572:69368572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.532A>G |
| AA Mutation | p.Ser178Gly(p.S178G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359426 |
| Start | 69384897:69384897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821G>T |
| AA Mutation | p.Gln607His(p.Q607H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359426 |
| Start | 69380057:69380057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367932087 |
| CDS Mutation | c.1227G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359426 |
| Start | 69392285:69392285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2196T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359426 |
| Start | 69364890:69364890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.483C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359426 |
| Start | 69384912:69384912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143834023 |
| CDS Mutation | c.1836C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000448642 |
| Start | 69288761:69288761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359426 |
| Start | 69377049:69377049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760487849 |
| CDS Mutation | c.991C>T |
| AA Mutation | p.Arg331Ter(p.R331*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |