Primary Site >> Stomach Cancer
Gene >> ZIC4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147390958:147390958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977C>T |
| AA Mutation | p.Ala326Val(p.A326V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396178:147396178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772620883 |
| CDS Mutation | c.362G>A |
| AA Mutation | p.Arg121His(p.R121H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396215:147396215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Ala109Thr(p.A109T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391205:147391205(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.730C>T |
| AA Mutation | p.Arg244Cys(p.R244C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396355:147396355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.185T>C |
| AA Mutation | p.Leu62Pro(p.L62P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391108:147391108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746281542 |
| CDS Mutation | c.827C>T |
| AA Mutation | p.Thr276Met(p.T276M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391207:147391207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.728G>A |
| AA Mutation | p.Arg243Gln(p.R243Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147395878:147395878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.662T>C |
| AA Mutation | p.Leu221Pro(p.L221P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396293:147396293(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.247G>A |
| AA Mutation | p.Ala83Thr(p.A83T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396051:147396051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.489C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147396303:147396303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.237G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391155:147391155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.780C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391212:147391212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780565526 |
| CDS Mutation | c.723C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147390996:147390996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.939C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383075 |
| Start | 147391170:147391170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369536221 |
| CDS Mutation | c.765G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |