Mutation

Primary Site >> Stomach Cancer

Gene >> FLT4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180613051:180613051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3391G>A
AA Mutation	p.Gly1131Ser(p.G1131S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180621661:180621661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1901C>T
AA Mutation	p.Ala634Val(p.A634V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180630235:180630235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148392893
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Met(p.T168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180630599:180630599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751885535
CDS Mutation	c.356G>A
AA Mutation	p.Arg119His(p.R119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180629397:180629397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368167894
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180630603:180630603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Ala118Ser(p.A118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180621658:180621658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904C>T
AA Mutation	p.Thr635Met(p.T635M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180620278:180620278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2437C>A
AA Mutation	p.Leu813Met(p.L813M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180625971:180625971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753074837
CDS Mutation	c.1319G>A
AA Mutation	p.Arg440His(p.R440H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180611423:180611423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3594C>G
AA Mutation	p.Ser1198Arg(p.S1198R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180628888:180628888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097T>C
AA Mutation	p.Phe366Ser(p.F366S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180629351:180629351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893A>G
AA Mutation	p.His298Arg(p.H298R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180626236:180626236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200763913
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180621800:180621800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1762C>A
AA Mutation	p.Leu588Met(p.L588M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180630684:180630684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Pro91Ser(p.P91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180619343:180619343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2671C>T
AA Mutation	p.Arg891Cys(p.R891C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180619728:180619728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2584G>A
AA Mutation	p.Ala862Thr(p.A862T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180621836:180621836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726C>A
AA Mutation	p.Leu576Met(p.L576M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261937
Start	180629346:180629346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186187161
CDS Mutation	c.898G>A
AA Mutation	p.Val300Ile(p.V300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180612518:180612518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3525C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180621190:180621190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180609920:180609920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3792C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180630790:180630790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781067773
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180620183:180620183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2532G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180618909:180618909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2862C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180620711:180620711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180621203:180621203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2070C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180621230:180621230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2043G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180603234:180603234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4050C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180630715:180630715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.240G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261937
Start	180630691:180630691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261937
Start	180631748:180631748(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.89delC
AA Mutation	p.Pro30ArgfsTer3(p.P30Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261937
Start	180628897:180628897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1088delC
AA Mutation	p.Pro363ArgfsTer27(p.P363Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261937
Start	180614131:180614137(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3262_3268delGACAAGG
AA Mutation	p.Asp1088CysfsTer39(p.D1088Cfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000261937
Start	180612544:180612544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3499G>T
AA Mutation	p.Glu1167Ter(p.E1167*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript