Primary Site >> Stomach Cancer
Gene >> TNS4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40496257:40496257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147274319 |
| CDS Mutation | c.169G>A |
| AA Mutation | p.Val57Met(p.V57M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40478584:40478584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368737342 |
| CDS Mutation | c.1975C>T |
| AA Mutation | p.Arg659Trp(p.R659W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40487417:40487417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.907T>A |
| AA Mutation | p.Ser303Thr(p.S303T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40484929:40484929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143122913 |
| CDS Mutation | c.1367G>A |
| AA Mutation | p.Arg456Gln(p.R456Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40496184:40496184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753848525 |
| CDS Mutation | c.242C>T |
| AA Mutation | p.Pro81Leu(p.P81L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40487409:40487409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.915A>C |
| AA Mutation | p.Arg305Ser(p.R305S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40487185:40487185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1139G>T |
| AA Mutation | p.Cys380Phe(p.C380F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40488846:40488846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764524983 |
| CDS Mutation | c.563G>C |
| AA Mutation | p.Arg188Thr(p.R188T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40482147:40482147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1654C>T |
| AA Mutation | p.Leu552Phe(p.L552F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000254051 |
| Start | 40487155:40487155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150836111 |
| CDS Mutation | c.1169G>A |
| AA Mutation | p.Arg390Gln(p.R390Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254051 |
| Start | 40485003:40485003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775924948 |
| CDS Mutation | c.1293C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000254051 |
| Start | 40478645:40478645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1914G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000254051 |
| Start | 40496337:40496343(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.83_89delTGCACCC |
| AA Mutation | p.Leu28GlnfsTer24(p.L28Qfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000254051 |
| Start | 40488964:40488964(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445A>T |
| AA Mutation | p.Lys149Ter(p.K149*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000254051 |
| Start | 40488835:40488835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146714186 |
| CDS Mutation | c.574C>T |
| AA Mutation | p.Arg192Ter(p.R192*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |