Mutation

Primary Site >> Stomach Cancer

Gene >> NR2F1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588274:93588274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93593768:93593768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198G>A
AA Mutation	p.Glu400Lys(p.E400K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588393:93588393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940G>A
AA Mutation	p.Val314Ile(p.V314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588127:93588127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674G>A
AA Mutation	p.Arg225His(p.R225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93585313:93585313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290A>G
AA Mutation	p.His97Arg(p.H97R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588422:93588422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969A>C
AA Mutation	p.Lys323Asn(p.K323N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588154:93588154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>G
AA Mutation	p.Ala234Gly(p.A234G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588144:93588144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Val231Ile(p.V231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588191:93588191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588038:93588038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588056:93588056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93593725:93593725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370092446
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93587993:93587993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747863258
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588432:93588432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588278:93588278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327111
Start	93587984:93587984(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.535delC
AA Mutation	p.Leu179SerfsTer178(p.L179Sfs*178)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000327111
Start	93593687:93593687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Ter(p.R373*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript