Primary Site >> Stomach Cancer
Gene >> CHD7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60853390:60853390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6665A>G |
| AA Mutation | p.Glu2222Gly(p.E2222G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60823984:60823984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3346A>G |
| AA Mutation | p.Lys1116Glu(p.K1116E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852169:60852169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5816G>A |
| AA Mutation | p.Arg1939Gln(p.R1939Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856752:60856752(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528722099 |
| CDS Mutation | c.7472G>A |
| AA Mutation | p.Arg2491His(p.R2491H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60844908:60844908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775776506 |
| CDS Mutation | c.4895G>A |
| AA Mutation | p.Arg1632His(p.R1632H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742829:60742829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs71640285 |
| CDS Mutation | c.1397C>T |
| AA Mutation | p.Ser466Leu(p.S466L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742292:60742292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.860C>T |
| AA Mutation | p.Pro287Leu(p.P287L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60800442:60800442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2293T>C |
| AA Mutation | p.Phe765Leu(p.F765L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865808:60865808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762553908 |
| CDS Mutation | c.8869G>A |
| AA Mutation | p.Asp2957Asn(p.D2957N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60836160:60836160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3866C>T |
| AA Mutation | p.Ala1289Val(p.A1289V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60836957:60836957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4130C>T |
| AA Mutation | p.Ala1377Val(p.A1377V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865029:60865029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8090A>G |
| AA Mutation | p.Glu2697Gly(p.E2697G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856533:60856533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761410781 |
| CDS Mutation | c.7253G>A |
| AA Mutation | p.Arg2418Gln(p.R2418Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742291:60742291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Pro287Ser(p.P287S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852094:60852094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5741G>A |
| AA Mutation | p.Arg1914His(p.R1914H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865292:60865292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8353G>A |
| AA Mutation | p.Ala2785Thr(p.A2785T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742507:60742507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1075C>G |
| AA Mutation | p.Gln359Glu(p.Q359E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741937:60741937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.505C>T |
| AA Mutation | p.Pro169Ser(p.P169S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742211:60742211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.779C>T |
| AA Mutation | p.Pro260Leu(p.P260L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742528:60742528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1096C>T |
| AA Mutation | p.Pro366Ser(p.P366S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741689:60741689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.257C>T |
| AA Mutation | p.Pro86Leu(p.P86L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865152:60865152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761409446 |
| CDS Mutation | c.8213C>T |
| AA Mutation | p.Thr2738Met(p.T2738M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60781015:60781015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1681C>A |
| AA Mutation | p.Pro561Thr(p.P561T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742783:60742783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1351G>A |
| AA Mutation | p.Gly451Ser(p.G451S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60853318:60853318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6593G>T |
| AA Mutation | p.Gly2198Val(p.G2198V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742180:60742180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368934543 |
| CDS Mutation | c.748C>T |
| AA Mutation | p.Arg250Cys(p.R250C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852883:60852883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6158G>A |
| AA Mutation | p.Arg2053Gln(p.R2053Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741521:60741521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768014298 |
| CDS Mutation | c.89C>T |
| AA Mutation | p.Pro30Leu(p.P30L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852937:60852937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6212A>G |
| AA Mutation | p.His2071Arg(p.H2071R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60781021:60781021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1687C>G |
| AA Mutation | p.Leu563Val(p.L563V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856502:60856502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7222G>A |
| AA Mutation | p.Glu2408Lys(p.E2408K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741677:60741677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.245T>C |
| AA Mutation | p.Leu82Pro(p.L82P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60830478:60830478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3679A>G |
| AA Mutation | p.Thr1227Ala(p.T1227A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60853355:60853355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6630G>T |
| AA Mutation | p.Glu2210Asp(p.E2210D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000423902 |
| Start | 60861097:60861097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7802A>G |
| AA Mutation | p.Tyr2601Cys(p.Y2601C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852833:60852833(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372755547 |
| CDS Mutation | c.6108G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741792:60741792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375438732 |
| CDS Mutation | c.360C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60850527:60850527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373869399 |
| CDS Mutation | c.5439C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865498:60865498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8559G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856816:60856816(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7536G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865465:60865465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8526A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60830510:60830510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372498366 |
| CDS Mutation | c.3711C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60781080:60781080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1746G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60830358:60830358(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3559T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60830555:60830555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3756C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60856484:60856484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7204A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741798:60741798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.366G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60852119:60852119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5766C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60742599:60742599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1167T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60845047:60845047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5034C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865690:60865690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761033941 |
| CDS Mutation | c.8751G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741516:60741516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.84T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000423902 |
| Start | 60861054:60861054(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7763delA |
| AA Mutation | p.Asn2588IlefsTer4(p.N2588Ifs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000423902 |
| Start | 60865895:60865895(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.8962delG |
| AA Mutation | p.Asp2988MetfsTer3(p.D2988Mfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000423902 |
| Start | 60741957:60741957(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.528delG |
| AA Mutation | p.Pro178LeufsTer33(p.P178Lfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000423902 |
| Start | 60853110:60853110(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.6389delA |
| AA Mutation | p.Asn2130ThrfsTer14(p.N2130Tfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000423902 |
| Start | 60822027:60822027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200220845 |
| CDS Mutation | c.2839C>T |
| AA Mutation | p.Arg947Ter(p.R947*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |