Mutation

Primary Site >> Stomach Cancer

Gene >> KIDINS220

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8778941:8778941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200104720
CDS Mutation	c.2569G>A
AA Mutation	p.Val857Ile(p.V857I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8733593:8733593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3904G>T
AA Mutation	p.Gly1302Cys(p.G1302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8786001:8786001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377758428
CDS Mutation	c.1969C>T
AA Mutation	p.Leu657Phe(p.L657F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8750161:8750161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3365G>T
AA Mutation	p.Ser1122Ile(p.S1122I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8730751:8730751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5285G>C
AA Mutation	p.Gly1762Ala(p.G1762A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8779015:8779015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2495A>T
AA Mutation	p.Asp832Val(p.D832V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8798257:8798257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.944C>T
AA Mutation	p.Ala315Val(p.A315V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8785796:8785796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572569622
CDS Mutation	c.2174G>A
AA Mutation	p.Arg725His(p.R725H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8790018:8790018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533098482
CDS Mutation	c.1483T>C
AA Mutation	p.Phe495Leu(p.F495L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8731309:8731309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202036173
CDS Mutation	c.4727C>T
AA Mutation	p.Ala1576Val(p.A1576V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8733593:8733593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538261513
CDS Mutation	c.3904G>A
AA Mutation	p.Gly1302Ser(p.G1302S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8803079:8803079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652T>C
AA Mutation	p.Ser218Pro(p.S218P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8751577:8751577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3079A>G
AA Mutation	p.Asn1027Asp(p.N1027D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8786256:8786256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889G>T
AA Mutation	p.Gly630Val(p.G630V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8751633:8751633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3023A>T
AA Mutation	p.Asn1008Ile(p.N1008I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8731111:8731111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769746944
CDS Mutation	c.4925G>A
AA Mutation	p.Arg1642Gln(p.R1642Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8731378:8731378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76169344
CDS Mutation	c.4658C>T
AA Mutation	p.Pro1553Leu(p.P1553L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8827086:8827086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8T>C
AA Mutation	p.Val3Ala(p.V3A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000256707
Start	8731225:8731225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761174681
CDS Mutation	c.4811C>T
AA Mutation	p.Ala1604Val(p.A1604V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256707
Start	8779134:8779134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2376A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256707
Start	8731662:8731662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4374C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256707
Start	8793901:8793901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256707
Start	8776842:8776842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776644704
CDS Mutation	c.2754C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256707
Start	8750253:8750253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778534103
CDS Mutation	c.3273G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256707
Start	8731619:8731619(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4417delC
AA Mutation	p.Leu1473TrpfsTer35(p.L1473Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256707
Start	8779098:8779098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2412delT
AA Mutation	p.Phe804LeufsTer9(p.F804Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256707
Start	8786010:8786010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1960delA
AA Mutation	p.Thr654HisfsTer34(p.T654Hfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000256707
Start	8817708:8817708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>A
AA Mutation	p.Trp72Ter(p.W72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256707
Start	8786009:8786010(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1960dupA
AA Mutation	p.Thr654AsnfsTer28(p.T654Nfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256707
Start	8731481:8731482(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4554dupA
AA Mutation	p.Leu1519ThrfsTer4(p.L1519Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	31
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000256707
Start	8806269:8806269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript