Primary Site >> Stomach Cancer

Gene >> CHD4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6591472:6591472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3334T>C
AA Mutation p.Phe1112Leu(p.F1112L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6599897:6599897(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1358G>A
AA Mutation p.Arg453Gln(p.R453Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6597955:6597955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1831C>T
AA Mutation p.Arg611Cys(p.R611C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6581323:6581323(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4747G>T
AA Mutation p.Val1583Phe(p.V1583F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6596055:6596055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1975G>A
AA Mutation p.Val659Met(p.V659M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6587885:6587885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3530G>A
AA Mutation p.Arg1177His(p.R1177H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6587930:6587930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3485G>A
AA Mutation p.Arg1162Gln(p.R1162Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6591492:6591492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3314G>A
AA Mutation p.Arg1105Gln(p.R1105Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6583253:6583253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4005A>C
AA Mutation p.Lys1335Asn(p.K1335N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6598349:6598349(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1559C>A
AA Mutation p.Pro520His(p.P520H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6578062:6578062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5195G>T
AA Mutation p.Arg1732Leu(p.R1732L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6582868:6582868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4216C>T
AA Mutation p.Arg1406Cys(p.R1406C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6577792:6577792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5354G>T
AA Mutation p.Arg1785Met(p.R1785M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6583245:6583245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4013G>T
AA Mutation p.Arg1338Ile(p.R1338I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6577904:6577904(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5242C>T
AA Mutation p.Arg1748Trp(p.R1748W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6583047:6583047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4127A>G
AA Mutation p.Asp1376Gly(p.D1376G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6592460:6592460(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2881G>A
AA Mutation p.Asp961Asn(p.D961N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6573233:6573233(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5398C>T
AA Mutation p.Arg1800Cys(p.R1800C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6593493:6593493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2437C>T
AA Mutation p.Arg813Cys(p.R813C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6578063:6578063(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767578728
CDS Mutation c.5194C>T
AA Mutation p.Arg1732Trp(p.R1732W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6587816:6587816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3599G>A
AA Mutation p.Arg1200Gln(p.R1200Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6583240:6583240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4018C>T
AA Mutation p.Arg1340Cys(p.R1340C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6577874:6577874(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5272T>C
AA Mutation p.Tyr1758His(p.Y1758H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6591927:6591927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3079G>A
AA Mutation p.Val1027Met(p.V1027M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6593114:6593114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2629C>T
AA Mutation p.Arg877Trp(p.R877W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6581702:6581702(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4628C>T
AA Mutation p.Pro1543Leu(p.P1543L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6592528:6592528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2813C>T
AA Mutation p.Ala938Val(p.A938V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6595341:6595341(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2114C>T
AA Mutation p.Thr705Ile(p.T705I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6578881:6578881(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4946C>T
AA Mutation p.Ala1649Val(p.A1649V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6587476:6587476(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3787G>A
AA Mutation p.Asp1263Asn(p.D1263N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6593492:6593492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2438G>A
AA Mutation p.Arg813His(p.R813H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6600584:6600584(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1013G>A
AA Mutation p.Arg338His(p.R338H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6594563:6594563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2209T>C
Mutation Classification Silent
Feature Type Transcript
ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6606311:6606311(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.63T>C
Mutation Classification Silent
Feature Type Transcript
ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6587486:6587486(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3777C>T
Mutation Classification Silent
Feature Type Transcript
ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6594588:6594588(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368003608
CDS Mutation c.2184C>T
Mutation Classification Silent
Feature Type Transcript
ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6591790:6591790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3126C>T
Mutation Classification Silent
Feature Type Transcript
ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6583070:6583070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4104G>T
Mutation Classification Silent
Feature Type Transcript
ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6592549:6592549(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2792delT
AA Mutation p.Leu931TrpfsTer13(p.L931Wfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 40
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6602380:6602380(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.218delA
AA Mutation p.Lys73ArgfsTer129(p.K73Rfs*129)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6599781:6599781(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1474delC
AA Mutation p.Arg492ValfsTer7(p.R492Vfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 42
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6606285:6606285(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.89delC
AA Mutation p.Pro30HisfsTer172(p.P30Hfs*172)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6578488:6578488(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5040delC
AA Mutation p.Lys1681ArgfsTer3(p.K1681Rfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 44
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6570951:6570952(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5638_5639delCC
AA Mutation p.Pro1880SerfsTer11(p.P1880Sfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 45
Mutation Consequence frameshift_variant
Transcription ID ENST00000357008
Start 6592506:6592506(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2835delA
AA Mutation p.Lys945AsnfsTer28(p.K945Nfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 46
Mutation Consequence stop_gained
Transcription ID ENST00000357008
Start 6582697:6582697(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4288C>T
AA Mutation p.Arg1430Ter(p.R1430*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript