Primary Site >> Stomach Cancer
Gene >> KIT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54736807:54736807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774405431 |
| CDS Mutation | c.2683G>A |
| AA Mutation | p.Ala895Thr(p.A895T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54695635:54695635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191T>C |
| AA Mutation | p.Val64Ala(p.V64A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54709464:54709464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1156G>A |
| AA Mutation | p.Glu386Lys(p.E386K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54736547:54736547(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2534T>C |
| AA Mutation | p.Val845Ala(p.V845A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54699763:54699763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.753T>G |
| AA Mutation | p.Ser251Arg(p.S251R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54658072:54658072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.58G>A |
| AA Mutation | p.Val20Ile(p.V20I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54695602:54695602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.158A>G |
| AA Mutation | p.Glu53Gly(p.E53G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54723667:54723667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1315G>C |
| AA Mutation | p.Asp439His(p.D439H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54658027:54658027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.13C>T |
| AA Mutation | p.Arg5Cys(p.R5C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54699666:54699666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.656C>G |
| AA Mutation | p.Ala219Gly(p.A219G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54707257:54707257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1085A>G |
| AA Mutation | p.Tyr362Cys(p.Y362C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288135 |
| Start | 54728057:54728057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1926A>C |
| AA Mutation | p.Lys642Asn(p.K642N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288135 |
| Start | 54703807:54703807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142772432 |
| CDS Mutation | c.840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288135 |
| Start | 54725974:54725974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1464G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288135 |
| Start | 54727908:54727908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200814065 |
| CDS Mutation | c.1860C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000288135 |
| Start | 54699764:54699765(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.755_756insCAGCTTTGAA |
| AA Mutation | p.Gln252HisfsTer6(p.Q252Hfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |