Primary Site >> Stomach Cancer
Gene >> PHIP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78946118:78946118(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4513C>G |
| AA Mutation | p.Arg1505Gly(p.R1505G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78945422:78945422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4706G>A |
| AA Mutation | p.Gly1569Asp(p.G1569D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79077495:79077495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.142C>T |
| AA Mutation | p.Arg48Cys(p.R48C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78966006:78966006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3256G>A |
| AA Mutation | p.Glu1086Lys(p.E1086K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79025564:79025564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.878G>A |
| AA Mutation | p.Gly293Asp(p.G293D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79016611:79016611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536256008 |
| CDS Mutation | c.1168C>T |
| AA Mutation | p.Arg390Cys(p.R390C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78997514:78997514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2101A>T |
| AA Mutation | p.Met701Leu(p.M701L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78997552:78997552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2063G>T |
| AA Mutation | p.Gly688Val(p.G688V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79015111:79015111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1495G>A |
| AA Mutation | p.Gly499Arg(p.G499R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79016626:79016626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1153C>T |
| AA Mutation | p.Arg385Cys(p.R385C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 79015200:79015200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406T>C |
| AA Mutation | p.Val469Ala(p.V469A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78954939:78954939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369513920 |
| CDS Mutation | c.3928C>T |
| AA Mutation | p.Arg1310Cys(p.R1310C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78958529:78958529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3728G>A |
| AA Mutation | p.Ser1243Asn(p.S1243N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000275034 |
| Start | 78998361:78998361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1910A>C |
| AA Mutation | p.Asn637Thr(p.N637T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 79042933:79042933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547487715 |
| CDS Mutation | c.510T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 78946818:78946818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4263T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 79003757:79003757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1626C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 78990880:78990880(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2307C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 79060536:79060536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376769294 |
| CDS Mutation | c.381G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 78985423:78985423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757432741 |
| CDS Mutation | c.2466C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000275034 |
| Start | 79017378:79017378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1104T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000275034 |
| Start | 79025548:79025548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.894G>A |
| AA Mutation | p.Trp298Ter(p.W298*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |