Primary Site >> Stomach Cancer
Gene >> HECTD4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112169592:112169592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11717C>T |
| AA Mutation | p.Ser3906Leu(p.S3906L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112273702:112273702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1463A>C |
| AA Mutation | p.Tyr488Ser(p.Y488S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112216917:112216917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761593797 |
| CDS Mutation | c.6839C>T |
| AA Mutation | p.Pro2280Leu(p.P2280L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112210114:112210114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7366G>A |
| AA Mutation | p.Ala2456Thr(p.A2456T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112231678:112231678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5633C>T |
| AA Mutation | p.Ala1878Val(p.A1878V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112273715:112273715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750765727 |
| CDS Mutation | c.1450C>G |
| AA Mutation | p.Gln484Glu(p.Q484E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112184897:112184897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747606994 |
| CDS Mutation | c.9667G>A |
| AA Mutation | p.Ala3223Thr(p.A3223T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163137:112163137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12623G>A |
| AA Mutation | p.Arg4208His(p.R4208H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112250174:112250174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370702531 |
| CDS Mutation | c.3518G>A |
| AA Mutation | p.Arg1173His(p.R1173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112212572:112212572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7142A>G |
| AA Mutation | p.Tyr2381Cys(p.Y2381C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112212584:112212584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7130A>G |
| AA Mutation | p.Lys2377Arg(p.K2377R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112235707:112235707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5120C>A |
| AA Mutation | p.Pro1707Gln(p.P1707Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112170375:112170375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746900553 |
| CDS Mutation | c.11608G>A |
| AA Mutation | p.Ala3870Thr(p.A3870T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112184915:112184915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9649A>G |
| AA Mutation | p.Met3217Val(p.M3217V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112229864:112229864(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5951T>G |
| AA Mutation | p.Leu1984Arg(p.L1984R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112183224:112183224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.10420T>A |
| AA Mutation | p.Phe3474Ile(p.F3474I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112193094:112193094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8651C>G |
| AA Mutation | p.Ser2884Cys(p.S2884C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112210044:112210044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7436G>A |
| AA Mutation | p.Arg2479Gln(p.R2479Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112231636:112231636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5675T>C |
| AA Mutation | p.Ile1892Thr(p.I1892T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112270387:112270387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1583T>A |
| AA Mutation | p.Leu528His(p.L528H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112184899:112184899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.9665G>A |
| AA Mutation | p.Arg3222His(p.R3222H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112279368:112279368(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764673654 |
| CDS Mutation | c.1115T>C |
| AA Mutation | p.Leu372Pro(p.L372P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112172763:112172763(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781440455 |
| CDS Mutation | c.11291G>A |
| AA Mutation | p.Arg3764His(p.R3764H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112254149:112254149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2909C>T |
| AA Mutation | p.Ala970Val(p.A970V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163111:112163111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.12649G>C |
| AA Mutation | p.Asp4217His(p.D4217H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163122:112163122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12638G>T |
| AA Mutation | p.Cys4213Phe(p.C4213F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112273672:112273672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1493T>G |
| AA Mutation | p.Ile498Ser(p.I498S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112243925:112243925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4196A>C |
| AA Mutation | p.Asp1399Ala(p.D1399A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112167438:112167438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12011C>T |
| AA Mutation | p.Pro4004Leu(p.P4004L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112184902:112184902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9662A>T |
| AA Mutation | p.His3221Leu(p.H3221L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112235140:112235140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5450T>C |
| AA Mutation | p.Leu1817Pro(p.L1817P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112243417:112243417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759425154 |
| CDS Mutation | c.4492G>A |
| AA Mutation | p.Val1498Ile(p.V1498I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112230808:112230808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5813G>A |
| AA Mutation | p.Arg1938His(p.R1938H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112243474:112243474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4435C>T |
| AA Mutation | p.Arg1479Trp(p.R1479W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112167522:112167522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11927C>A |
| AA Mutation | p.Thr3976Asn(p.T3976N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112229768:112229768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200891866 |
| CDS Mutation | c.6047G>A |
| AA Mutation | p.Arg2016His(p.R2016H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112250252:112250252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3440C>A |
| AA Mutation | p.Pro1147His(p.P1147H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112200713:112200713(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8090G>T |
| AA Mutation | p.Arg2697Met(p.R2697M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112212563:112212563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7151A>G |
| AA Mutation | p.Tyr2384Cys(p.Y2384C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112194900:112194900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745915493 |
| CDS Mutation | c.8332G>A |
| AA Mutation | p.Ala2778Thr(p.A2778T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000550722 |
| Start | 112185113:112185113(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9451G>A |
| AA Mutation | p.Ala3151Thr(p.A3151T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112200670:112200670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8133C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112192717:112192717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775434958 |
| CDS Mutation | c.8733C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112258591:112258591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752347793 |
| CDS Mutation | c.2601G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112283237:112283237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368428068 |
| CDS Mutation | c.969C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112208524:112208524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778274507 |
| CDS Mutation | c.7572C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112216916:112216916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376336161 |
| CDS Mutation | c.6840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 48 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112235723:112235723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5104C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 49 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112250215:112250215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 50 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112252436:112252436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3138A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 51 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112212559:112212559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 52 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000550722 |
| Start | 112184898:112184898(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 53 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163201:112163201(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.12559delG |
| AA Mutation | p.Ala4187ProfsTer44(p.A4187Pfs*44) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 54 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163056:112163056(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs746492036 |
| CDS Mutation | c.12704delC |
| AA Mutation | p.Pro4235GlnfsTer21(p.P4235Qfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 55 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112252545:112252545(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3029delC |
| AA Mutation | p.Pro1010LeufsTer3(p.P1010Lfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 56 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000550722 |
| Start | 112237027:112237027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4960C>T |
| AA Mutation | p.Arg1654Ter(p.R1654*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 57 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000550722 |
| Start | 112219484:112219484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6574C>T |
| AA Mutation | p.Arg2192Ter(p.R2192*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 58 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112163055:112163056(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs774893697 |
| CDS Mutation | c.12704dupC |
| AA Mutation | p.Asp4236ArgfsTer44(p.D4236Rfs*44) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 59 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112247041:112247042(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3963_3970dupTCTTATTC |
| AA Mutation | p.Gln1324LeufsTer16(p.Q1324Lfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 60 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000550722 |
| Start | 112176602:112176603(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.11061dupA |
| AA Mutation | p.Gln3688ThrfsTer5(p.Q3688Tfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |