Primary Site >> Stomach Cancer
Gene >> PHKA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18908871:18908871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2290G>C |
| AA Mutation | p.Val764Leu(p.V764L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18954403:18954403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.88A>G |
| AA Mutation | p.Thr30Ala(p.T30A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18940045:18940045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868C>T |
| AA Mutation | p.Arg290Cys(p.R290C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18895146:18895146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3328A>G |
| AA Mutation | p.Thr1110Ala(p.T1110A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18920163:18920163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1832C>T |
| AA Mutation | p.Ser611Leu(p.S611L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18894364:18894364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3377C>T |
| AA Mutation | p.Ser1126Leu(p.S1126L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18943798:18943798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.629A>G |
| AA Mutation | p.Glu210Gly(p.E210G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18931663:18931663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1223T>C |
| AA Mutation | p.Ile408Thr(p.I408T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18951224:18951224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.334C>A |
| AA Mutation | p.Leu112Met(p.L112M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18906501:18906501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2800T>C |
| AA Mutation | p.Cys934Arg(p.C934R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18905802:18905802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2864T>C |
| AA Mutation | p.Leu955Pro(p.L955P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000379942 |
| Start | 18936055:18936055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1137G>T |
| AA Mutation | p.Lys379Asn(p.K379N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18908900:18908900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2261A>G |
| AA Mutation | p.Asp754Gly(p.D754G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379942 |
| Start | 18894271:18894271(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3470G>T |
| AA Mutation | p.Ser1157Ile(p.S1157I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379942 |
| Start | 18894288:18894288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747924699 |
| CDS Mutation | c.3453G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379942 |
| Start | 18894297:18894297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774402125 |
| CDS Mutation | c.3444G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379942 |
| Start | 18901581:18901581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2931A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379942 |
| Start | 18894345:18894345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374048049 |
| CDS Mutation | c.3396G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |