Primary Site >> Stomach Cancer
Gene >> KEAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10489291:10489291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1609T>C |
| AA Mutation | p.Tyr537His(p.Y537H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499885:10499885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149G>A |
| AA Mutation | p.Arg50His(p.R50H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10492156:10492156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.746G>A |
| AA Mutation | p.Cys249Tyr(p.C249Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499900:10499900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134C>T |
| AA Mutation | p.Ser45Phe(p.S45F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10491970:10491970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932A>G |
| AA Mutation | p.His311Arg(p.H311R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499782:10499782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.252G>C |
| AA Mutation | p.Lys84Asn(p.K84N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000171111 |
| Start | 10492262:10492262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.640G>A |
| AA Mutation | p.Val214Met(p.V214M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10489278:10489278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1622C>T |
| AA Mutation | p.Thr541Ile(p.T541I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10492040:10492040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.862T>C |
| AA Mutation | p.Cys288Arg(p.C288R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499934:10499934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372654184 |
| CDS Mutation | c.100G>A |
| AA Mutation | p.Ala34Thr(p.A34T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000171111 |
| Start | 10486712:10486712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139000421 |
| CDS Mutation | c.1815C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499800:10499800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771599341 |
| CDS Mutation | c.234C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499749:10499749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.285C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499416:10499416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000171111 |
| Start | 10499590:10499590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11545828 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |