Mutation

Primary Site >> Stomach Cancer

Gene >> LRRN2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619241:204619241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369686045
CDS Mutation	c.752G>A
AA Mutation	p.Arg251Gln(p.R251Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618110:204618110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142606457
CDS Mutation	c.1883G>A
AA Mutation	p.Arg628His(p.R628H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618602:204618602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771218431
CDS Mutation	c.1391G>A
AA Mutation	p.Arg464Gln(p.R464Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618773:204618773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749764096
CDS Mutation	c.1220C>T
AA Mutation	p.Pro407Leu(p.P407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618972:204618972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021A>G
AA Mutation	p.Met341Val(p.M341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619712:204619712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281A>G
AA Mutation	p.Asn94Ser(p.N94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619803:204619803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
AA Mutation	p.Pro64Ser(p.P64S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618645:204618645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762590445
CDS Mutation	c.1348G>A
AA Mutation	p.Glu450Lys(p.E450K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204618768:204618768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141763834
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Cys(p.R409C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619346:204619346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143481345
CDS Mutation	c.647G>A
AA Mutation	p.Arg216His(p.R216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619746:204619746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778124325
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Cys(p.R83C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619238:204619238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755T>C
AA Mutation	p.Val252Ala(p.V252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619932:204619932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.61C>T
AA Mutation	p.Pro21Ser(p.P21S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367175
Start	204619305:204619305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139753603
CDS Mutation	c.688G>A
AA Mutation	p.Asp230Asn(p.D230N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204619849:204619849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781709899
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204619599:204619599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204617944:204617944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573586615
CDS Mutation	c.2049T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204618085:204618085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1908T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204618052:204618052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375246174
CDS Mutation	c.1941G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204619675:204619675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367175
Start	204619243:204619243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749849276
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367175
Start	204618701:204618701(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1292delC
AA Mutation	p.Pro431GlnfsTer5(p.P431Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367175
Start	204619789:204619789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.204delC
AA Mutation	p.Ala69GlnfsTer52(p.A69Qfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000367175
Start	204618359:204618359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1634G>A
AA Mutation	p.Trp545Ter(p.W545*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript