Primary Site >> Stomach Cancer
Gene >> CHD9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53156897:53156897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.808T>A |
| AA Mutation | p.Phe270Ile(p.F270I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53242951:53242951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2989G>A |
| AA Mutation | p.Asp997Asn(p.D997N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53238527:53238527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2818G>T |
| AA Mutation | p.Gly940Trp(p.G940W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53209546:53209546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1517G>T |
| AA Mutation | p.Arg506Met(p.R506M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53324376:53324376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8175G>T |
| AA Mutation | p.Leu2725Phe(p.L2725F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53156819:53156819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.730T>C |
| AA Mutation | p.Cys244Arg(p.C244R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53157000:53157000(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911A>C |
| AA Mutation | p.Asp304Ala(p.D304A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53318255:53318255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7628G>A |
| AA Mutation | p.Arg2543His(p.R2543H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53267426:53267426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4453G>A |
| AA Mutation | p.Asp1485Asn(p.D1485N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53245728:53245728(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3332G>A |
| AA Mutation | p.Arg1111Gln(p.R1111Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53324099:53324099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370913156 |
| CDS Mutation | c.7898G>A |
| AA Mutation | p.Arg2633Gln(p.R2633Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53157300:53157300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1211T>G |
| AA Mutation | p.Leu404Arg(p.L404R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53242963:53242963(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3001A>G |
| AA Mutation | p.Arg1001Gly(p.R1001G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53157308:53157308(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147266259 |
| CDS Mutation | c.1219G>A |
| AA Mutation | p.Glu407Lys(p.E407K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53297131:53297131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5686A>G |
| AA Mutation | p.Arg1896Gly(p.R1896G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53307834:53307834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6934G>A |
| AA Mutation | p.Asp2312Asn(p.D2312N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53238386:53238386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2677A>G |
| AA Mutation | p.Ile893Val(p.I893V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53156334:53156334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.245T>C |
| AA Mutation | p.Val82Ala(p.V82A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53209734:53209734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1705A>T |
| AA Mutation | p.Arg569Trp(p.R569W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53297110:53297110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs563054232 |
| CDS Mutation | c.5665G>A |
| AA Mutation | p.Ala1889Thr(p.A1889T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000398510 |
| Start | 53324123:53324123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7922C>T |
| AA Mutation | p.Ala2641Val(p.A2641V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398510 |
| Start | 53287987:53287987(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5220C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398510 |
| Start | 53268101:53268101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4692G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398510 |
| Start | 53156707:53156707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754207747 |
| CDS Mutation | c.618T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398510 |
| Start | 53209520:53209520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000398510 |
| Start | 53324136:53324136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7935A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53324090:53324090(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7893delG |
| AA Mutation | p.Arg2632AspfsTer28(p.R2632Dfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53229088:53229088(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.2280delT |
| AA Mutation | p.Phe760LeufsTer16(p.F760Lfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53285610:53285610(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4984delG |
| AA Mutation | p.Val1662TyrfsTer87(p.V1662Yfs*87) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53292931:53292931(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5393delA |
| AA Mutation | p.Asn1798ThrfsTer17(p.N1798Tfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53314439:53314439(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748826986 |
| CDS Mutation | c.7291delA |
| AA Mutation | p.Arg2431GlyfsTer8(p.R2431Gfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000398510 |
| Start | 53242911:53242911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2949T>A |
| AA Mutation | p.Cys983Ter(p.C983*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53318242:53318243(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.7621dupA |
| AA Mutation | p.Arg2541LysfsTer9(p.R2541Kfs*9) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000398510 |
| Start | 53209570:53209571(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs772443637 |
| CDS Mutation | c.1547dupA |
| AA Mutation | p.Val517GlyfsTer11(p.V517Gfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000398510 |
| Start | 53235184:53235184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2512-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |