Primary Site >> Stomach Cancer
Gene >> TBC1D1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38045869:38045869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1595G>A |
| AA Mutation | p.Ser532Asn(p.S532N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38133174:38133174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3223A>G |
| AA Mutation | p.Ser1075Gly(p.S1075G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38014785:38014785(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.694A>G |
| AA Mutation | p.Met232Val(p.M232V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38137149:38137149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3321G>C |
| AA Mutation | p.Arg1107Ser(p.R1107S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38044419:38044419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1471T>G |
| AA Mutation | p.Phe491Val(p.F491V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000261439 |
| Start | 38044489:38044489(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772487620 |
| CDS Mutation | c.1541G>A |
| AA Mutation | p.Arg514Gln(p.R514Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38137298:38137298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3470A>T |
| AA Mutation | p.Glu1157Val(p.E1157V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38049823:38049823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779792096 |
| CDS Mutation | c.1835G>A |
| AA Mutation | p.Arg612Gln(p.R612Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38118130:38118130(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2900C>T |
| AA Mutation | p.Ala967Val(p.A967V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261439 |
| Start | 38021650:38021650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1142A>G |
| AA Mutation | p.Lys381Arg(p.K381R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38020638:38020638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182769159 |
| CDS Mutation | c.1020C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38049833:38049833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528041274 |
| CDS Mutation | c.1845G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38014658:38014658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.567G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38054313:38054313(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369081896 |
| CDS Mutation | c.2025G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38014892:38014892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746363297 |
| CDS Mutation | c.801C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38014670:38014670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.579C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261439 |
| Start | 38137161:38137161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3333T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261439 |
| Start | 38096064:38096064(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2377delA |
| AA Mutation | p.Met793CysfsTer21(p.M793Cfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261439 |
| Start | 38054290:38054290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775294678 |
| CDS Mutation | c.2002C>T |
| AA Mutation | p.Arg668Ter(p.R668*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261439 |
| Start | 38044436:38044437(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1493dupA |
| AA Mutation | p.Asn498LysfsTer19(p.N498Kfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |