Primary Site >> Stomach Cancer
Gene >> ZFYVE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72993318:72993318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754283630 |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Arg343Gln(p.R343Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72993174:72993174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759215529 |
| CDS Mutation | c.1172G>A |
| AA Mutation | p.Arg391Gln(p.R391Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72974134:72974134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2047G>A |
| AA Mutation | p.Glu683Lys(p.E683K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72974940:72974940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757171387 |
| CDS Mutation | c.1826C>T |
| AA Mutation | p.Thr609Met(p.T609M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72993175:72993175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765009506 |
| CDS Mutation | c.1171C>T |
| AA Mutation | p.Arg391Trp(p.R391W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000556143 |
| Start | 72997976:72997976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.823G>A |
| AA Mutation | p.Asp275Asn(p.D275N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000556143 |
| Start | 72974939:72974939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751442684 |
| CDS Mutation | c.1827G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000556143 |
| Start | 72998097:72998097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762124006 |
| CDS Mutation | c.702C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |