Primary Site >> Stomach Cancer
Gene >> ZIC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412662:147412662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1127C>T |
| AA Mutation | p.Ser376Leu(p.S376L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410698:147410698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764570223 |
| CDS Mutation | c.586G>A |
| AA Mutation | p.Gly196Ser(p.G196S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412527:147412527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.992C>T |
| AA Mutation | p.Pro331Leu(p.P331L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410524:147410524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412G>A |
| AA Mutation | p.Ala138Thr(p.A138T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410236:147410236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.124G>A |
| AA Mutation | p.Asp42Asn(p.D42N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410371:147410371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259G>A |
| AA Mutation | p.Gly87Ser(p.G87S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410873:147410873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.761C>T |
| AA Mutation | p.Thr254Met(p.T254M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410378:147410378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.266A>C |
| AA Mutation | p.Tyr89Ser(p.Y89S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410345:147410345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Gly78Asp(p.G78D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410728:147410728(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 | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147411055:147411055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.943C>T |
| AA Mutation | p.Arg315Cys(p.R315C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412565:147412565(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1030G>A |
| AA Mutation | p.Ala344Thr(p.A344T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410437:147410437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Asp109Asn(p.D109N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412668:147412668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1133G>A |
| AA Mutation | p.Arg378His(p.R378H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410615:147410615(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Ser168Leu(p.S168L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410734:147410734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.622C>A |
| AA Mutation | p.His208Asn(p.H208N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410825:147410825(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713C>A |
| AA Mutation | p.Pro238His(p.P238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410528:147410528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.416G>A |
| AA Mutation | p.Gly139Asp(p.G139D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410942:147410942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.830C>T |
| AA Mutation | p.Pro277Leu(p.P277L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410688:147410688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759778746 |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410286:147410286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755293143 |
| CDS Mutation | c.174G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412537:147412537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1002C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410727:147410727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410496:147410496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.384C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410577:147410577(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410958:147410958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.846C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410523:147410523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750080738 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147410169:147410169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756393471 |
| CDS Mutation | c.57G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282928 |
| Start | 147412636:147412636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777958545 |
| CDS Mutation | c.1101C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |