Primary Site >> Stomach Cancer
Gene >> IRF4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 401655:401655(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201105575 |
| CDS Mutation | c.977C>T |
| AA Mutation | p.Ala326Val(p.A326V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 393249:393249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.97G>A |
| AA Mutation | p.Asp33Asn(p.D33N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 395910:395910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755460615 |
| CDS Mutation | c.467C>T |
| AA Mutation | p.Thr156Met(p.T156M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 405036:405036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1118A>G |
| AA Mutation | p.His373Arg(p.H373R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 394831:394831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227T>C |
| AA Mutation | p.Leu76Pro(p.L76P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 401458:401458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.780A>C |
| AA Mutation | p.Glu260Asp(p.E260D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 398884:398884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375133421 |
| CDS Mutation | c.694G>A |
| AA Mutation | p.Gly232Arg(p.G232R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380956 |
| Start | 397237:397237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.622C>T |
| AA Mutation | p.Pro208Ser(p.P208S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 401485:401485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777806353 |
| CDS Mutation | c.807C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 405052:405052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1134G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 401689:401689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774672138 |
| CDS Mutation | c.1011C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 401701:401701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202225254 |
| CDS Mutation | c.1023G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 398832:398832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.642C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 394997:394997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.393A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 394868:394868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380956 |
| Start | 401656:401656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766676957 |
| CDS Mutation | c.978G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |