Mutation

Primary Site >> Stomach Cancer

Gene >> FBXW7

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152326137:152326137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149680468
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Cys(p.R505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152326214:152326214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436G>A
AA Mutation	p.Arg479Gln(p.R479Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152328233:152328233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1393C>T
AA Mutation	p.Arg465Cys(p.R465C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152411763:152411763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200698994
CDS Mutation	c.41G>A
AA Mutation	p.Arg14Gln(p.R14Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152326150:152326150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1500T>A
AA Mutation	p.His500Gln(p.H500Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152328232:152328232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394G>A
AA Mutation	p.Arg465His(p.R465H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152322984:152322984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021G>A
AA Mutation	p.Arg674Gln(p.R674Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152326206:152326206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1444A>T
AA Mutation	p.Thr482Ser(p.T482S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152323129:152323129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876G>A
AA Mutation	p.Ala626Thr(p.A626T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000281708
Start	152337803:152337803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860A>T
AA Mutation	p.Glu287Val(p.E287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152329698:152329698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210A>G
AA Mutation	p.Lys404Glu(p.K404E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152326208:152326208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000281708
Start	152411782:152411782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22G>A
AA Mutation	p.Val8Met(p.V8M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281708
Start	152322913:152322913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757047739
CDS Mutation	c.2092C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281708
Start	152324362:152324362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1677T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281708
Start	152346938:152346938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.718delA
AA Mutation	p.Met240CysfsTer14(p.M240Cfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281708
Start	152323004:152323004(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2001delG
AA Mutation	p.Ser668ValfsTer39(p.S668Vfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000281708
Start	152328209:152328209(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1417delA
AA Mutation	p.Arg473GlufsTer25(p.R473Efs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281708
Start	152326205:152326205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1445delC
AA Mutation	p.Thr482IlefsTer16(p.T482Ifs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000281708
Start	152330782:152330782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>T
AA Mutation	p.Gln358Ter(p.Q358*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000281708
Start	152326015:152326015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635T>G
AA Mutation	p.Tyr545Ter(p.Y545*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000281708
Start	152337831:152337831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Ter(p.R278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000281708
Start	152324187:152324187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852C>T
AA Mutation	p.Gln618Ter(p.Q618*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000281708
Start	152328208:152328209(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1417dupA
AA Mutation	p.Arg473LysfsTer4(p.R473Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281708
Start	152322962:152322963(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2042dupA
AA Mutation	p.Leu682AlafsTer12(p.L682Afs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281708
Start	152330833:152330834(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1020dupA
AA Mutation	p.Val341SerfsTer22(p.V341Sfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000281708
Start	152350040:152350040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript