Mutation

Primary Site >> Stomach Cancer

Gene >> CTCF

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67636803:67636803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762060506
CDS Mutation	c.1951C>T
AA Mutation	p.Arg651Trp(p.R651W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67620791:67620791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181T>C
AA Mutation	p.Leu394Pro(p.L394P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67612007:67612007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838A>C
AA Mutation	p.Asn280His(p.N280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67626648:67626648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1451A>C
AA Mutation	p.Gln484Pro(p.Q484P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67611577:67611577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747052464
CDS Mutation	c.745A>G
AA Mutation	p.Met249Val(p.M249V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67628506:67628506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655C>A
AA Mutation	p.Pro552His(p.P552H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67616808:67616808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67628397:67628397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546A>G
AA Mutation	p.Thr516Ala(p.T516A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264010
Start	67628465:67628465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779124853
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264010
Start	67616773:67616773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67637752:67637752(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2070delA
AA Mutation	p.Glu691SerfsTer30(p.E691Sfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611436:67611436(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.610delA
AA Mutation	p.Thr204GlnfsTer18(p.T204Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67621578:67621578(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs34679888
CDS Mutation	c.1348delA
AA Mutation	p.Ser450ValfsTer61(p.S450Vfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67612033:67612033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.864delC
AA Mutation	p.His288GlnfsTer22(p.H288Qfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000264010
Start	67626713:67626713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516C>T
AA Mutation	p.Gln506Ter(p.Q506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611372:67611373(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.544dupG
AA Mutation	p.Glu182GlyfsTer9(p.E182Gfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611435:67611436(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.610dupA
AA Mutation	p.Thr204AsnfsTer26(p.T204Nfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611435:67611436(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.609_610dupAA
AA Mutation	p.Thr204LysfsTer19(p.T204Kfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67637751:67637752(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2070dupA
AA Mutation	p.Glu691ArgfsTer5(p.E691Rfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264010
Start	67626716:67626716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript