Primary Site >> Stomach Cancer
Gene >> DUSP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110498185:110498185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.64C>T |
| AA Mutation | p.Arg22Cys(p.R22C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110510385:110510385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1114G>A |
| AA Mutation | p.Glu372Lys(p.E372K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110498330:110498330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755076416 |
| CDS Mutation | c.209C>T |
| AA Mutation | p.Ala70Val(p.A70V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110506987:110506987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.581C>T |
| AA Mutation | p.Ala194Val(p.A194V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110510121:110510121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.850T>G |
| AA Mutation | p.Phe284Val(p.F284V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369583 |
| Start | 110498180:110498180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372205197 |
| CDS Mutation | c.59C>T |
| AA Mutation | p.Ala20Val(p.A20V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369583 |
| Start | 110498136:110498136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777773018 |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |