Primary Site >> Stomach Cancer
Gene >> FLT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28004152:28004152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2882G>C |
| AA Mutation | p.Arg961Pro(p.R961P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28048296:28048296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1184A>G |
| AA Mutation | p.Lys395Arg(p.K395R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28018499:28018499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2509A>C |
| AA Mutation | p.Met837Leu(p.M837L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28004071:28004071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2963C>A |
| AA Mutation | p.Ala988Asp(p.A988D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28034172:28034172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767430269 |
| CDS Mutation | c.1747G>A |
| AA Mutation | p.Gly583Ser(p.G583S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28034117:28034117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1802T>C |
| AA Mutation | p.Leu601Pro(p.L601P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28061996:28061996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.239C>T |
| AA Mutation | p.Ala80Val(p.A80V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28062048:28062048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.187C>A |
| AA Mutation | p.Leu63Ile(p.L63I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28048439:28048439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1041G>T |
| AA Mutation | p.Lys347Asn(p.K347N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28035983:28035983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1370A>G |
| AA Mutation | p.Tyr457Cys(p.Y457C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241453 |
| Start | 28023376:28023376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2392G>A |
| AA Mutation | p.Gly798Arg(p.G798R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241453 |
| Start | 28062037:28062037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752191320 |
| CDS Mutation | c.198G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241453 |
| Start | 28034134:28034134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748696886 |
| CDS Mutation | c.1785A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000241453 |
| Start | 28052619:28052619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs56033040 |
| CDS Mutation | c.540C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |