Primary Site >> Stomach Cancer
Gene >> ZNF70
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23744054:23744054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201651839 |
| CDS Mutation | c.1087C>T |
| AA Mutation | p.Pro363Ser(p.P363S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23744251:23744251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201324895 |
| CDS Mutation | c.890G>A |
| AA Mutation | p.Arg297Gln(p.R297Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23745131:23745131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10C>T |
| AA Mutation | p.Pro4Ser(p.P4S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23743919:23743919(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143352353 |
| CDS Mutation | c.1222G>A |
| AA Mutation | p.Glu408Lys(p.E408K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23743940:23743940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781342377 |
| CDS Mutation | c.1201C>T |
| AA Mutation | p.Arg401Trp(p.R401W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000341976 |
| Start | 23743978:23743978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1163G>A |
| AA Mutation | p.Gly388Asp(p.G388D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000341976 |
| Start | 23744469:23744469(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758069065 |
| CDS Mutation | c.672C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |