Primary Site >> Stomach Cancer
Gene >> HNRNPK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83970225:83970225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1298G>T |
| AA Mutation | p.Arg433Leu(p.R433L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83970283:83970283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1240C>T |
| AA Mutation | p.Arg414Cys(p.R414C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83970903:83970903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1102G>A |
| AA Mutation | p.Gly368Arg(p.G368R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83970225:83970225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1298G>A |
| AA Mutation | p.Arg433Gln(p.R433Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83971943:83971943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760176912 |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Gly298Ser(p.G298S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351839 |
| Start | 83972098:83972098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.737G>C |
| AA Mutation | p.Arg246Pro(p.R246P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351839 |
| Start | 83972145:83972145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200783060 |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |