Primary Site >> Stomach Cancer
Gene >> JRK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612905 |
| Start | 142664563:142664563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781926968 |
| CDS Mutation | c.1496G>A |
| AA Mutation | p.Arg499His(p.R499H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612905 |
| Start | 142665811:142665811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782347045 |
| CDS Mutation | c.248C>T |
| AA Mutation | p.Thr83Met(p.T83M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612905 |
| Start | 142664607:142664607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782626920 |
| CDS Mutation | c.1452G>T |
| AA Mutation | p.Glu484Asp(p.E484D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612905 |
| Start | 142664635:142664635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17846351 |
| CDS Mutation | c.1424G>A |
| AA Mutation | p.Gly475Asp(p.G475D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000612905 |
| Start | 142664707:142664707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587679068 |
| CDS Mutation | c.1352G>A |
| AA Mutation | p.Arg451Gln(p.R451Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612905 |
| Start | 142665879:142665879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782439628 |
| CDS Mutation | c.180G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612905 |
| Start | 142665825:142665825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.234G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000612905 |
| Start | 142665897:142665897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.162C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000612905 |
| Start | 142664901:142664901(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782111957 |
| CDS Mutation | c.1158G>A |
| AA Mutation | p.Trp386Ter(p.W386*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |