Mutation

Primary Site >> Stomach Cancer

Gene >> KL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33016891:33016891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451A>T
AA Mutation	p.Ile151Phe(p.I151F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33054007:33054007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060G>A
AA Mutation	p.Glu354Lys(p.E354K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33053920:33053920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973G>T
AA Mutation	p.Gly325Cys(p.G325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33017194:33017194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Cys(p.R252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33060773:33060773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694C>T
AA Mutation	p.Thr565Ile(p.T565I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33016843:33016843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Asp135Asn(p.D135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33054046:33054046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761383989
CDS Mutation	c.1099T>G
AA Mutation	p.Phe367Val(p.F367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33017057:33017057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.617G>A
AA Mutation	p.Gly206Asp(p.G206D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33017122:33017122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>A
AA Mutation	p.Gly228Ser(p.G228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33017068:33017068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33055064:33055064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348G>A
AA Mutation	p.Val450Met(p.V450M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33017179:33017179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Gly247Ser(p.G247S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33064038:33064038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2891C>A
AA Mutation	p.Pro964Gln(p.P964Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33016960:33016960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Trp(p.R174W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000380099
Start	33061249:33061249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2170G>A
AA Mutation	p.Gly724Arg(p.G724R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33016848:33016848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33061710:33061710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138004650
CDS Mutation	c.2631C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33016854:33016854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33016953:33016953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33061119:33061119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138723796
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33016689:33016689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772081828
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33017046:33017046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33016782:33016782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753373810
CDS Mutation	c.342G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380099
Start	33061767:33061767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145682430
CDS Mutation	c.2688C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380099
Start	33061457:33061457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2384delA
AA Mutation	p.Lys795SerfsTer2(p.K795Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380099
Start	33064069:33064069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2928delT
AA Mutation	p.His977ThrfsTer10(p.H977Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380099
Start	33064068:33064069(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2928dupT
AA Mutation	p.His977SerfsTer83(p.H977Sfs*83)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript