Mutation

Primary Site >> Stomach Cancer

Gene >> LINGO2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949674:27949674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376500553
CDS Mutation	c.998T>C
AA Mutation	p.Leu333Pro(p.L333P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950350:27950350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778347323
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Cys(p.R108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949195:27949195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477A>G
AA Mutation	p.Thr493Ala(p.T493A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27948866:27948866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1806C>A
AA Mutation	p.Asn602Lys(p.N602K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949743:27949743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559778213
CDS Mutation	c.929G>A
AA Mutation	p.Arg310His(p.R310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950149:27950149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>A
AA Mutation	p.Gly175Arg(p.G175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949662:27949662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010A>G
AA Mutation	p.Glu337Gly(p.E337G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949140:27949140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532C>T
AA Mutation	p.Ala511Val(p.A511V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950386:27950386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>A
AA Mutation	p.Val96Met(p.V96M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949049:27949049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1623A>G
AA Mutation	p.Ile541Met(p.I541M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950092:27950092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580A>G
AA Mutation	p.Thr194Ala(p.T194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950592:27950592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80G>T
AA Mutation	p.Gly27Val(p.G27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950157:27950157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>A
AA Mutation	p.Ala172Glu(p.A172E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949500:27949500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172G>A
AA Mutation	p.Arg391Lys(p.R391K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27950417:27950417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255G>T
AA Mutation	p.Glu85Asp(p.E85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949435:27949435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237C>T
AA Mutation	p.Arg413Cys(p.R413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949807:27949807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Glu289Lys(p.E289K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000308675
Start	27949153:27949153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780715183
CDS Mutation	c.1519C>T
AA Mutation	p.Arg507Cys(p.R507C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27949673:27949673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27949055:27949055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27949358:27949358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200772912
CDS Mutation	c.1314G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27950567:27950567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27949700:27949700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138682295
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308675
Start	27950159:27950159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308675
Start	27948948:27948948(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1724delA
AA Mutation	p.Asn575ThrfsTer21(p.N575Tfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000308675
Start	27949025:27949025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1647C>A
AA Mutation	p.Cys549Ter(p.C549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308675
Start	27949444:27949445(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1227dupA
AA Mutation	p.Pro410ThrfsTer5(p.P410Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript