Primary Site >> Stomach Cancer
Gene >> PHKA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72581097:72581097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3577C>G |
| AA Mutation | p.Pro1193Ala(p.P1193A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72593159:72593159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3188C>T |
| AA Mutation | p.Ala1063Val(p.A1063V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72581133:72581133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140865522 |
| CDS Mutation | c.3541G>A |
| AA Mutation | p.Ala1181Thr(p.A1181T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72581163:72581163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144813238 |
| CDS Mutation | c.3511G>A |
| AA Mutation | p.Ala1171Thr(p.A1171T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72582486:72582486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3410T>C |
| AA Mutation | p.Leu1137Pro(p.L1137P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72609691:72609691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2539C>G |
| AA Mutation | p.Leu847Val(p.L847V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72653442:72653442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1130C>T |
| AA Mutation | p.Pro377Leu(p.P377L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000373542 |
| Start | 72644362:72644362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1459G>A |
| AA Mutation | p.Gly487Arg(p.G487R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72581021:72581021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3653G>A |
| AA Mutation | p.Ser1218Asn(p.S1218N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72636356:72636356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1490G>A |
| AA Mutation | p.Arg497Gln(p.R497Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373542 |
| Start | 72611143:72611143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2411C>T |
| AA Mutation | p.Ala804Val(p.A804V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373542 |
| Start | 72611121:72611121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61732499 |
| CDS Mutation | c.2433C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373542 |
| Start | 72712794:72712794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.222C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373542 |
| Start | 72713857:72713857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.24G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373542 |
| Start | 72676145:72676145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781909169 |
| CDS Mutation | c.543C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |