Mutation

Primary Site >> Stomach Cancer

Gene >> NRG1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764076:32764076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597C>T
AA Mutation	p.Pro533Ser(p.P533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764233:32764233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754A>G
AA Mutation	p.Asp585Gly(p.D585G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32595909:32595909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182C>A
AA Mutation	p.Ser61Tyr(p.S61Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756413:32756413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814A>G
AA Mutation	p.Lys272Glu(p.K272E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000523534
Start	31640515:31640515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>T
AA Mutation	p.Lys30Asn(p.K30N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764348:32764348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1869A>C
AA Mutation	p.Glu623Asp(p.E623D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764161:32764161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1682A>C
AA Mutation	p.Glu561Ala(p.E561A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32756447:32756447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145033301
CDS Mutation	c.848G>A
AA Mutation	p.Arg283Gln(p.R283Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000523534
Start	31640660:31640660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235T>C
AA Mutation	p.Ser79Pro(p.S79P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32614541:32614541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>T
AA Mutation	p.Thr143Ile(p.T143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764020:32764020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541C>T
AA Mutation	p.Ala514Val(p.A514V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32764295:32764295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147189312
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Cys(p.R606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763771:32763771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753126752
CDS Mutation	c.1292C>T
AA Mutation	p.Pro431Leu(p.P431L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763996:32763996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572301736
CDS Mutation	c.1517C>T
AA Mutation	p.Ala506Val(p.A506V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000405005
Start	32763938:32763938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145066694
CDS Mutation	c.1459C>T
AA Mutation	p.Arg487Trp(p.R487W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000523534
Start	31640569:31640569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32760209:32760209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114135581
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32760293:32760293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32605586:32605586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32595949:32595949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32760284:32760284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1146C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32760233:32760233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772910330
CDS Mutation	c.1095C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000405005
Start	32763994:32763994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000405005
Start	32595993:32595993(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.272delA
AA Mutation	p.Lys91SerfsTer24(p.K91Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000405005
Start	32742018:32742018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>T
AA Mutation	p.Gly215Ter(p.G215*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000405005
Start	32764343:32764343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1864G>T
AA Mutation	p.Glu622Ter(p.E622*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript