Primary Site >> Stomach Cancer
Gene >> FBXO24
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100600731:100600731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1575G>T |
| AA Mutation | p.Gln525His(p.Q525H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100595594:100595594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1094G>A |
| AA Mutation | p.Gly365Asp(p.G365D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100590044:100590044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778850634 |
| CDS Mutation | c.107C>T |
| AA Mutation | p.Pro36Leu(p.P36L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100592857:100592857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.633A>C |
| AA Mutation | p.Glu211Asp(p.E211D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100600562:100600562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406C>A |
| AA Mutation | p.Ala469Asp(p.A469D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100592991:100592991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.767C>A |
| AA Mutation | p.Thr256Asn(p.T256N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100595677:100595677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1177G>A |
| AA Mutation | p.Asp393Asn(p.D393N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100594410:100594410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.821T>C |
| AA Mutation | p.Val274Ala(p.V274A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100595197:100595197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1048C>T |
| AA Mutation | p.Pro350Ser(p.P350S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100590279:100590279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.244A>G |
| AA Mutation | p.Ile82Val(p.I82V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000241071 |
| Start | 100591871:100591871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768402143 |
| CDS Mutation | c.527G>A |
| AA Mutation | p.Arg176His(p.R176H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000241071 |
| Start | 100595106:100595106(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.962delG |
| AA Mutation | p.Gly321GlufsTer69(p.G321Efs*69) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000241071 |
| Start | 100595105:100595106(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.962dupG |
| AA Mutation | p.Val322SerfsTer4(p.V322Sfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |