Primary Site >> Stomach Cancer
Gene >> ZNFX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270403:49270403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1409C>G |
| AA Mutation | p.Ser470Cys(p.S470C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49271520:49271520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.292G>T |
| AA Mutation | p.Asp98Tyr(p.D98Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270419:49270419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1393C>A |
| AA Mutation | p.Leu465Ile(p.L465I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49254585:49254585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377053417 |
| CDS Mutation | c.2869C>T |
| AA Mutation | p.Arg957Cys(p.R957C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270265:49270265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1547G>T |
| AA Mutation | p.Arg516Met(p.R516M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49247451:49247451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757387154 |
| CDS Mutation | c.5573G>A |
| AA Mutation | p.Gly1858Asp(p.G1858D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49257500:49257500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2581G>A |
| AA Mutation | p.Ala861Thr(p.A861T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49249438:49249438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781451100 |
| CDS Mutation | c.3586C>A |
| AA Mutation | p.Leu1196Ile(p.L1196I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270524:49270524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1288G>C |
| AA Mutation | p.Val430Leu(p.V430L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000371752 |
| Start | 49264862:49264862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2005A>G |
| AA Mutation | p.Ile669Val(p.I669V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270445:49270445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1367T>C |
| AA Mutation | p.Met456Thr(p.M456T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49248037:49248037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150988771 |
| CDS Mutation | c.4987C>T |
| AA Mutation | p.Arg1663Trp(p.R1663W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49271087:49271087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.725A>T |
| AA Mutation | p.Glu242Val(p.E242V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49270751:49270751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761250796 |
| CDS Mutation | c.1061G>A |
| AA Mutation | p.Arg354His(p.R354H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49248219:49248219(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773563724 |
| CDS Mutation | c.4805G>A |
| AA Mutation | p.Arg1602His(p.R1602H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371752 |
| Start | 49251606:49251606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3233A>C |
| AA Mutation | p.Glu1078Ala(p.E1078A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371752 |
| Start | 49248701:49248701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775867313 |
| CDS Mutation | c.4323C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371752 |
| Start | 49249430:49249430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146287599 |
| CDS Mutation | c.3594G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371752 |
| Start | 49263397:49263397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2238A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371752 |
| Start | 49249568:49249568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3456C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371752 |
| Start | 49248055:49248055(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4969delA |
| AA Mutation | p.Ile1657Ter(p.I1657*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371752 |
| Start | 49255845:49255845(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2767delT |
| AA Mutation | p.Trp923GlyfsTer44(p.W923Gfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371752 |
| Start | 49249586:49249586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3438C>A |
| AA Mutation | p.Cys1146Ter(p.C1146*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371752 |
| Start | 49257584:49257584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2497C>T |
| AA Mutation | p.Gln833Ter(p.Q833*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000371752 |
| Start | 49271103:49271103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772546721 |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Ter(p.R237*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371752 |
| Start | 49255913:49255914(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2698dupA |
| AA Mutation | p.Arg900LysfsTer5(p.R900Kfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000371752 |
| Start | 49255927:49255928(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2684dupA |
| AA Mutation | p.Lys896GlufsTer9(p.K896Efs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000371752 |
| Start | 49251525:49251525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3312+2T>G |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |