Primary Site >> Stomach Cancer
Gene >> HK3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176881117:176881117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756312063 |
| CDS Mutation | c.2728G>T |
| AA Mutation | p.Val910Phe(p.V910F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176881173:176881173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2672G>A |
| AA Mutation | p.Arg891His(p.R891H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176884095:176884095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1897G>T |
| AA Mutation | p.Asp633Tyr(p.D633Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887585:176887585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1466C>T |
| AA Mutation | p.Pro489Leu(p.P489L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887296:176887296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1642T>C |
| AA Mutation | p.Phe548Leu(p.F548L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176881390:176881390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762226493 |
| CDS Mutation | c.2539G>A |
| AA Mutation | p.Val847Met(p.V847M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176881993:176881993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780234736 |
| CDS Mutation | c.2188C>T |
| AA Mutation | p.Arg730Cys(p.R730C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887513:176887513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769496471 |
| CDS Mutation | c.1538G>A |
| AA Mutation | p.Arg513Gln(p.R513Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887552:176887552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1499T>G |
| AA Mutation | p.Val500Gly(p.V500G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292432 |
| Start | 176881330:176881330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2599G>A |
| AA Mutation | p.Asp867Asn(p.D867N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887231:176887231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1707C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176890897:176890897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146938667 |
| CDS Mutation | c.459G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176882123:176882123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771884359 |
| CDS Mutation | c.2058C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176883831:176883831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554140413 |
| CDS Mutation | c.1992G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887249:176887249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201110208 |
| CDS Mutation | c.1689C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176887264:176887264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141954469 |
| CDS Mutation | c.1674C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292432 |
| Start | 176884090:176884090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114856191 |
| CDS Mutation | c.1902C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |