Primary Site >> Stomach Cancer
Gene >> HIPK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369558 |
| Start | 113954655:113954655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1205G>A |
| AA Mutation | p.Arg402His(p.R402H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369558 |
| Start | 113970190:113970190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3006G>T |
| AA Mutation | p.Gln1002His(p.Q1002H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369558 |
| Start | 113973165:113973165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3286C>A |
| AA Mutation | p.Pro1096Thr(p.P1096T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369558 |
| Start | 113941413:113941413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs192499620 |
| CDS Mutation | c.1030G>A |
| AA Mutation | p.Val344Ile(p.V344I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369558 |
| Start | 113940975:113940975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Trp(p.R198W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369558 |
| Start | 113970187:113970187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3003C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369558 |
| Start | 113940410:113940410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577913437 |
| CDS Mutation | c.27G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369558 |
| Start | 113940659:113940659(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.276G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369558 |
| Start | 113941358:113941358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.975T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369558 |
| Start | 113957277:113957277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1746G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369558 |
| Start | 113940456:113940456(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.76delA |
| AA Mutation | p.Ile26Ter(p.I26*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369558 |
| Start | 113954723:113954723(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1277delT |
| AA Mutation | p.Phe426SerfsTer26(p.F426Sfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369558 |
| Start | 113973444:113973444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758110661 |
| CDS Mutation | c.3565C>T |
| AA Mutation | p.Arg1189Ter(p.R1189*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |