Primary Site >> Stomach Cancer
Gene >> KCNH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150958340:150958340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.635T>C |
| AA Mutation | p.Leu212Pro(p.L212P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951783:150951783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs794728373 |
| CDS Mutation | c.1610G>A |
| AA Mutation | p.Arg537Gln(p.R537Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150959598:150959598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199472865 |
| CDS Mutation | c.446G>C |
| AA Mutation | p.Gly149Ala(p.G149A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951109:150951109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1957G>A |
| AA Mutation | p.Ala653Thr(p.A653T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951813:150951813(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580C>T |
| AA Mutation | p.Ala527Val(p.A527V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951828:150951828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778103101 |
| CDS Mutation | c.1565G>A |
| AA Mutation | p.Gly522Glu(p.G522E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150977870:150977870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.44T>C |
| AA Mutation | p.Leu15Pro(p.L15P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951772:150951772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764666519 |
| CDS Mutation | c.1621C>T |
| AA Mutation | p.Arg541Cys(p.R541C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262186 |
| Start | 150948897:150948897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2551C>G |
| AA Mutation | p.His851Asp(p.H851D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150950933:150950933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2133C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150957447:150957447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146297032 |
| CDS Mutation | c.972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951758:150951758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200692436 |
| CDS Mutation | c.1635C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150951812:150951812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150275982 |
| CDS Mutation | c.1581G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262186 |
| Start | 150950190:150950190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745993706 |
| CDS Mutation | c.2376C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000262186 |
| Start | 150959591:150959591(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767521596 |
| CDS Mutation | c.453delC |
| AA Mutation | p.Thr152ProfsTer14(p.T152Pfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |