Primary Site >> Stomach Cancer
Gene >> NOD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50710645:50710645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148516118 |
| CDS Mutation | c.734C>T |
| AA Mutation | p.Thr245Met(p.T245M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50699860:50699860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.446T>C |
| AA Mutation | p.Val149Ala(p.V149A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711460:50711460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1549A>G |
| AA Mutation | p.Ile517Val(p.I517V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50725546:50725546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2940G>T |
| AA Mutation | p.Lys980Asn(p.K980N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50722628:50722628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2721G>T |
| AA Mutation | p.Trp907Cys(p.W907C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000300589 |
| Start | 50699488:50699488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567793250 |
| CDS Mutation | c.74G>A |
| AA Mutation | p.Gly25Asp(p.G25D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711698:50711698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142077546 |
| CDS Mutation | c.1787C>T |
| AA Mutation | p.Thr596Met(p.T596M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711989:50711989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2078G>A |
| AA Mutation | p.Cys693Tyr(p.C693Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50729849:50729849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2998G>T |
| AA Mutation | p.Ala1000Ser(p.A1000S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300589 |
| Start | 50699854:50699854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776403451 |
| CDS Mutation | c.440G>A |
| AA Mutation | p.Ser147Asn(p.S147N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50710718:50710718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369766454 |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711690:50711690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771570437 |
| CDS Mutation | c.1779A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711864:50711864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1953C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50712152:50712152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751417475 |
| CDS Mutation | c.2241C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300589 |
| Start | 50699504:50699504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774491311 |
| CDS Mutation | c.90G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711488:50711488(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs757534831 |
| CDS Mutation | c.1583delC |
| AA Mutation | p.Pro528GlnfsTer235(p.P528Qfs*235) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000300589 |
| Start | 50711420:50711420(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs767278572 |
| CDS Mutation | c.1515delG |
| AA Mutation | p.Ser506ProfsTer11(p.S506Pfs*11) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |