Primary Site >> Stomach Cancer
Gene >> ZIC3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137570055:137570055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1389C>A |
| AA Mutation | p.Asn463Lys(p.N463K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567591:137567591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.900G>T |
| AA Mutation | p.Glu300Asp(p.E300D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567697:137567697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1006G>A |
| AA Mutation | p.Gly336Arg(p.G336R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567307:137567307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.616C>T |
| AA Mutation | p.Arg206Cys(p.R206C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567103:137567103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412G>A |
| AA Mutation | p.Gly138Arg(p.G138R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567260:137567260(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.569G>T |
| AA Mutation | p.Gly190Val(p.G190V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137570059:137570059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393T>C |
| AA Mutation | p.Trp465Arg(p.W465R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287538 |
| Start | 137567560:137567560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752160420 |
| CDS Mutation | c.869C>T |
| AA Mutation | p.Pro290Leu(p.P290L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287538 |
| Start | 137568936:137568936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1095T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287538 |
| Start | 137568939:137568939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1098C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287538 |
| Start | 137569020:137569020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754070677 |
| CDS Mutation | c.1179C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |