Mutation

Primary Site >> Stomach Cancer

Gene >> REV3L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111376254:111376254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101A>G
AA Mutation	p.Thr701Ala(p.T701A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111376651:111376651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704A>T
AA Mutation	p.Glu568Asp(p.E568D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111374106:111374106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4249C>T
AA Mutation	p.Pro1417Ser(p.P1417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111375623:111375623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2732G>A
AA Mutation	p.Gly911Glu(p.G911E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111329617:111329617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376298082
CDS Mutation	c.8156C>T
AA Mutation	p.Ala2719Val(p.A2719V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111374984:111374984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3371C>T
AA Mutation	p.Ser1124Phe(p.S1124F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111333214:111333214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375272662
CDS Mutation	c.7834G>A
AA Mutation	p.Val2612Ile(p.V2612I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111373274:111373274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5081A>C
AA Mutation	p.Asn1694Thr(p.N1694T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111358939:111358939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6955G>T
AA Mutation	p.Asp2319Tyr(p.D2319Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111373604:111373604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776259034
CDS Mutation	c.4751G>A
AA Mutation	p.Arg1584Gln(p.R1584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111374306:111374306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4049A>G
AA Mutation	p.Glu1350Gly(p.E1350G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111373076:111373076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5279A>T
AA Mutation	p.Asp1760Val(p.D1760V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111374900:111374900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3455G>A
AA Mutation	p.Gly1152Asp(p.G1152D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111375159:111375159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3196A>G
AA Mutation	p.Asn1066Asp(p.N1066D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111358931:111358931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6963C>G
AA Mutation	p.Ile2321Met(p.I2321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111333321:111333321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7727A>T
AA Mutation	p.Tyr2576Phe(p.Y2576F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111375192:111375192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3163G>T
AA Mutation	p.Ala1055Ser(p.A1055S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111367741:111367741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199592368
CDS Mutation	c.6047A>G
AA Mutation	p.Tyr2016Cys(p.Y2016C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111309993:111309993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140606020
CDS Mutation	c.8902C>T
AA Mutation	p.Arg2968Cys(p.R2968C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111375384:111375384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2971C>A
AA Mutation	p.Leu991Ile(p.L991I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111311249:111311249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374701728
CDS Mutation	c.8615G>A
AA Mutation	p.Arg2872His(p.R2872H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111307440:111307440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766889673
CDS Mutation	c.9173G>A
AA Mutation	p.Arg3058Gln(p.R3058Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111367829:111367829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5959G>A
AA Mutation	p.Val1987Ile(p.V1987I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111333231:111333231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747486955
CDS Mutation	c.7817A>G
AA Mutation	p.Tyr2606Cys(p.Y2606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111315319:111315319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8414C>T
AA Mutation	p.Ala2805Val(p.A2805V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111381397:111381397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1144A>G
AA Mutation	p.Ile382Val(p.I382V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111374201:111374201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4154A>T
AA Mutation	p.Asn1385Ile(p.N1385I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111372861:111372861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768017978
CDS Mutation	c.5494G>A
AA Mutation	p.Val1832Met(p.V1832M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111389157:111389157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764659947
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Trp(p.R271W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111380163:111380163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273G>A
AA Mutation	p.Gly425Arg(p.G425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111329629:111329629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141338934
CDS Mutation	c.8144G>A
AA Mutation	p.Arg2715Gln(p.R2715Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111367627:111367627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750229185
CDS Mutation	c.6161A>G
AA Mutation	p.Asp2054Gly(p.D2054G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111343988:111343988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578253914
CDS Mutation	c.7475G>A
AA Mutation	p.Arg2492His(p.R2492H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000358835
Start	111365284:111365284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6734T>C
AA Mutation	p.Val2245Ala(p.V2245A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111363907:111363907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6825T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111375976:111375976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2379A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111375517:111375517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2838T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111367740:111367740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753982547
CDS Mutation	c.6048C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111322673:111322673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145957765
CDS Mutation	c.8247C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111372862:111372862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201671524
CDS Mutation	c.5493C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111331730:111331730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7980T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111375870:111375870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2485C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358835
Start	111374644:111374644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3711T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111367814:111367814(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5974delA
AA Mutation	p.Ile1992LeufsTer2(p.I1992Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111388045:111388045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.903delT
AA Mutation	p.Gln302ArgfsTer15(p.Q302Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	46
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111374905:111374905(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3450delT
AA Mutation	p.Phe1150LeufsTer15(p.F1150Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	47
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111405616:111405616(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.419delT
AA Mutation	p.Leu140CysfsTer6(p.L140Cfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	48
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111374096:111374096(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4259delT
AA Mutation	p.Leu1420CysfsTer13(p.L1420Cfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111376375:111376375(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1980delT
AA Mutation	p.Phe660LeufsTer53(p.F660Lfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111367429:111367429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6359delC
AA Mutation	p.Pro2120LeufsTer5(p.P2120Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111335508:111335508(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7641delT
AA Mutation	p.Phe2547LeufsTer9(p.F2547Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111379985:111379985(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1451delA
AA Mutation	p.Lys484ArgfsTer33(p.K484Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	stop_gained
Transcription ID	ENST00000358835
Start	111374775:111374775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3580C>T
AA Mutation	p.Arg1194Ter(p.R1194*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111375736:111375737(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2618dupT
AA Mutation	p.Leu873PhefsTer3(p.L873Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111388047:111388048(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.900dupA
AA Mutation	p.Phe301IlefsTer13(p.F301Ifs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111376696:111376697(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1658_1659insGTCTGTGAAAGGTC
AA Mutation	p.Pro557GlyfsTer16(p.P557Gfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111367813:111367814(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.5974dupA
AA Mutation	p.Ile1992AsnfsTer33(p.I1992Nfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358835
Start	111367592:111367593(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6195dupT
AA Mutation	p.Thr2066TyrfsTer6(p.T2066Yfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	59
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000358835
Start	111365261:111365266(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6752_6753+4delAGGTAA
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	60
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000358835
Start	111387914:111387914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript