Primary Site >> Stomach Cancer
Gene >> BTBD7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93251552:93251552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1853C>T |
| AA Mutation | p.Ala618Val(p.A618V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294308:93294308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143569452 |
| CDS Mutation | c.712C>T |
| AA Mutation | p.Arg238Cys(p.R238C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93242601:93242601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368457475 |
| CDS Mutation | c.3071C>T |
| AA Mutation | p.Pro1024Leu(p.P1024L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294842:93294842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.178A>G |
| AA Mutation | p.Thr60Ala(p.T60A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294269:93294269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Leu251Phe(p.L251F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294044:93294044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781110720 |
| CDS Mutation | c.976A>G |
| AA Mutation | p.Thr326Ala(p.T326A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294292:93294292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.728A>G |
| AA Mutation | p.Tyr243Cys(p.Y243C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93245878:93245878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2530A>G |
| AA Mutation | p.Thr844Ala(p.T844A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294118:93294118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902A>G |
| AA Mutation | p.Glu301Gly(p.E301G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000334746 |
| Start | 93251550:93251550(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374714816 |
| CDS Mutation | c.1855G>A |
| AA Mutation | p.Val619Met(p.V619M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334746 |
| Start | 93257207:93257207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1596C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294903:93294903(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765663061 |
| CDS Mutation | c.117C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334746 |
| Start | 93296046:93296046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000334746 |
| Start | 93251572:93251572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758817668 |
| CDS Mutation | c.1833G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93242669:93242669(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3003delA |
| AA Mutation | p.Lys1001AsnfsTer60(p.K1001Nfs*60) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294156:93294156(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.864delT |
| AA Mutation | p.Arg289GlufsTer19(p.R289Efs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93263838:93263838(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1318delT |
| AA Mutation | p.Tyr440MetfsTer28(p.Y440Mfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294847:93294847(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752512017 |
| CDS Mutation | c.173delA |
| AA Mutation | p.Lys58ArgfsTer44(p.K58Rfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93242668:93242669(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs762347380 |
| CDS Mutation | c.3003dupA |
| AA Mutation | p.Gln1002ThrfsTer5(p.Q1002Tfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93242874:93242875(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2797dupA |
| AA Mutation | p.Thr933AsnfsTer15(p.T933Nfs*15) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93253701:93253702(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1697dupA |
| AA Mutation | p.Asn566LysfsTer24(p.N566Kfs*24) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000334746 |
| Start | 93294518:93294519(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.501dupT |
| AA Mutation | p.Lys168Ter(p.K168*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |