Mutation

Primary Site >> Stomach Cancer

Gene >> NFX1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379540
Start	33318815:33318815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673T>C
AA Mutation	p.Leu558Ser(p.L558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379540
Start	33301350:33301350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1121G>T
AA Mutation	p.Cys374Phe(p.C374F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379540
Start	33294872:33294872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478G>A
AA Mutation	p.Gly160Ser(p.G160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379540
Start	33295209:33295209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815C>T
AA Mutation	p.Ala272Val(p.A272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379540
Start	33307205:33307205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282A>C
AA Mutation	p.Asn428His(p.N428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33295423:33295423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33319099:33319099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773080677
CDS Mutation	c.1878C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33351733:33351733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748822455
CDS Mutation	c.2598G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33294679:33294679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777875408
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33295162:33295162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33294994:33294994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747975920
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379540
Start	33369966:33369966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201337993
CDS Mutation	c.3351C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379540
Start	33294467:33294467(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.80delA
AA Mutation	p.Asn27IlefsTer4(p.N27Ifs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379540
Start	33294846:33294848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.454_456delTCT
AA Mutation	p.Ser152del(p.S152del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379540
Start	33366763:33366768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3176_3181delCTGCCA
AA Mutation	p.Thr1059_Ala1060del(p.T1059_A1060del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript