Mutation

Primary Site >> Stomach Cancer

Gene >> PHF8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	53939241:53939241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3100C>T
AA Mutation	p.Arg1034Cys(p.R1034C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	54011130:54011130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1046T>C
AA Mutation	p.Ile349Thr(p.I349T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	54017670:54017670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>T
AA Mutation	p.His185Tyr(p.H185Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	53992806:53992806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1768G>A
AA Mutation	p.Asp590Asn(p.D590N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	53999887:53999887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324G>T
AA Mutation	p.Ala442Ser(p.A442S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	54011260:54011260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782033442
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	54016700:54016700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200His(p.R200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	53993620:53993620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715G>C
AA Mutation	p.Gly572Ala(p.G572A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	54002158:54002158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Cys(p.R416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357988
Start	53987786:53987786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997C>T
AA Mutation	p.Ala666Val(p.A666V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357988
Start	53987848:53987848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782251598
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357988
Start	54011144:54011144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357988
Start	54042699:54042699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357988
Start	53985073:53985073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2392C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357988
Start	54022318:54022318(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.342delA
AA Mutation	p.Lys114AsnfsTer3(p.K114Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357988
Start	53995691:53995691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript