Primary Site >> Stomach Cancer
Gene >> ZDHHC14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157672779:157672779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370693708 |
| CDS Mutation | c.1124C>T |
| AA Mutation | p.Thr375Met(p.T375M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157672738:157672738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1083G>T |
| AA Mutation | p.Gln361His(p.Q361H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157542608:157542608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.269T>A |
| AA Mutation | p.Ile90Asn(p.I90N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157542684:157542684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.345C>A |
| AA Mutation | p.Ser115Arg(p.S115R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157593020:157593020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.439C>T |
| AA Mutation | p.Arg147Cys(p.R147C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157632842:157632842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.712C>A |
| AA Mutation | p.Gln238Lys(p.Q238K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157382236:157382236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.215T>G |
| AA Mutation | p.Leu72Arg(p.L72R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359775 |
| Start | 157653614:157653614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1055C>T |
| AA Mutation | p.Ser352Leu(p.S352L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359775 |
| Start | 157645791:157645791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756023797 |
| CDS Mutation | c.807A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000359775 |
| Start | 157628444:157628445(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.662_663delCA |
| AA Mutation | p.Thr221SerfsTer25(p.T221Sfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |