Mutation

Primary Site >> Stomach Cancer

Gene >> LRIG1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66417144:66417144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146856805
CDS Mutation	c.488C>T
AA Mutation	p.Pro163Leu(p.P163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66384063:66384063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548930200
CDS Mutation	c.1999G>A
AA Mutation	p.Ala667Thr(p.A667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66414929:66414929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638T>C
AA Mutation	p.Leu213Pro(p.L213P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66405238:66405238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120A>G
AA Mutation	p.Thr374Ala(p.T374A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66407411:66407411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Ser339Asn(p.S339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66384014:66384014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2048C>A
AA Mutation	p.Ala683Asp(p.A683D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66417195:66417195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437T>G
AA Mutation	p.Leu146Arg(p.L146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66386277:66386277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493T>C
AA Mutation	p.Ile498Thr(p.I498T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66383342:66383342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131G>A
AA Mutation	p.Ala711Thr(p.A711T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66383200:66383200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146697512
CDS Mutation	c.2273C>T
AA Mutation	p.Ala758Val(p.A758V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66385998:66385998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1772C>T
AA Mutation	p.Ala591Val(p.A591V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66386238:66386238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532A>G
AA Mutation	p.Asp511Gly(p.D511G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66413003:66413003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66380286:66380286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3259C>G
AA Mutation	p.Leu1087Val(p.L1087V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66380359:66380359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767537467
CDS Mutation	c.3186C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66381573:66381573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2676C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66380326:66380326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371148346
CDS Mutation	c.3219G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66417245:66417245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775148095
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66398165:66398165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780001736
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66407458:66407458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534184911
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66384028:66384028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2034C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66380290:66380290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369456584
CDS Mutation	c.3255G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273261
Start	66384089:66384089(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1973delT
AA Mutation	p.Phe658SerfsTer5(p.F658Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000273261
Start	66386284:66386284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486C>T
AA Mutation	p.Gln496Ter(p.Q496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript