Primary Site >> Stomach Cancer
Gene >> TNKS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91819540:91819540(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.616G>A |
| AA Mutation | p.Ala206Thr(p.A206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91862988:91862988(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3490G>A |
| AA Mutation | p.Val1164Ile(p.V1164I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91831119:91831119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1213C>T |
| AA Mutation | p.His405Tyr(p.H405Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91842365:91842365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2033G>C |
| AA Mutation | p.Arg678Thr(p.R678T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91851263:91851263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2742G>T |
| AA Mutation | p.Glu914Asp(p.E914D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91859606:91859606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3239G>A |
| AA Mutation | p.Gly1080Glu(p.G1080E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371627 |
| Start | 91848384:91848384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758827793 |
| CDS Mutation | c.2360C>T |
| AA Mutation | p.Ala787Val(p.A787V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91840676:91840676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764051162 |
| CDS Mutation | c.1643A>G |
| AA Mutation | p.His548Arg(p.H548R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371627 |
| Start | 91857528:91857528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3092A>G |
| AA Mutation | p.His1031Arg(p.H1031R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371627 |
| Start | 91840606:91840606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755266752 |
| CDS Mutation | c.1573C>T |
| AA Mutation | p.Arg525Cys(p.R525C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371627 |
| Start | 91822326:91822326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.759T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371627 |
| Start | 91842342:91842342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2010A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371627 |
| Start | 91849591:91849591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2691A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371627 |
| Start | 91842189:91842189(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749004712 |
| CDS Mutation | c.1865delA |
| AA Mutation | p.Asn622ThrfsTer29(p.N622Tfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371627 |
| Start | 91828320:91828320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1018C>T |
| AA Mutation | p.Arg340Ter(p.R340*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371627 |
| Start | 91851240:91851241(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2720dupT |
| AA Mutation | p.Met907IlefsTer17(p.M907Ifs*17) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |