Colon Cancer: Gene >> CTCF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67616826:67616826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034A>G
AA Mutation	p.His345Arg(p.H345R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67628421:67628421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767996920
CDS Mutation	c.1570G>A
AA Mutation	p.Ala524Thr(p.A524T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67610917:67610917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771567232
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Trp(p.R29W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67620739:67620739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Arg377Cys(p.R377C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67626677:67626677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480C>T
AA Mutation	p.Arg494Cys(p.R494C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67612001:67612001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Cys(p.R278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67628406:67628406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Gly519Arg(p.G519R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67620712:67620712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102C>T
AA Mutation	p.Arg368Cys(p.R368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67626704:67626704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507G>T
AA Mutation	p.Ala503Ser(p.A503S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67629503:67629503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775874494
CDS Mutation	c.1807C>T
AA Mutation	p.Arg603Cys(p.R603C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67626587:67626587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>A
AA Mutation	p.Glu464Lys(p.E464K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264010
Start	67628420:67628420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761420338
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
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

Mutation ID	14
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

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611016:67611029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.184_197delATGATGGAACAGCT
AA Mutation	p.Met62GlyfsTer10(p.M62Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000264010
Start	67611610:67611610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778A>T
AA Mutation	p.Lys260Ter(p.K260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation 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

Mutation ID	18
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

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264010
Start	67611406:67611407(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.579dupA
AA Mutation	p.Asp194ArgfsTer36(p.D194Rfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000264010
Start	67611184:67611201(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.361_378delCCTGTGACTGTACCTGTT
AA Mutation	p.Pro121_Val126del(p.P121_V126del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTCF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67620722:67620722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67610903:67610903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71C>G
AA Mutation	p.Thr24Ser(p.T24S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67636785:67636785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1933C>T
AA Mutation	p.Pro645Ser(p.P645S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67616807:67616807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Trp(p.R339W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67610851:67610851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779609208
CDS Mutation	c.19G>A
AA Mutation	p.Glu7Lys(p.E7K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264010
Start	67629503:67629503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775874494
CDS Mutation	c.1807C>T
AA Mutation	p.Arg603Cys(p.R603C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript