Mutation

Primary Site >> Stomach Cancer

Gene >> HNF4A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44406222:44406222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280T>C
AA Mutation	p.Tyr94His(p.Y94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44413765:44413765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457A>G
AA Mutation	p.Asn153Asp(p.N153D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44406114:44406114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376906221
CDS Mutation	c.172G>A
AA Mutation	p.Ala58Thr(p.A58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44428448:44428448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757897768
CDS Mutation	c.1243G>A
AA Mutation	p.Gly415Arg(p.G415R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44419780:44419780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796A>G
AA Mutation	p.Ile266Val(p.I266V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44429597:44429597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776824742
CDS Mutation	c.1357G>A
AA Mutation	p.Val453Ile(p.V453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316099
Start	44428343:44428343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138A>G
AA Mutation	p.Ser380Gly(p.S380G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316099
Start	44406176:44406176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753302065
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316099
Start	44428447:44428447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141448616
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316099
Start	44418500:44418500(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.724delG
AA Mutation	p.Val242CysfsTer4(p.V242Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000316099
Start	44428469:44428469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264C>T
AA Mutation	p.Arg422Ter(p.R422*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript