Colon Cancer: Gene >> TCF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134142819:134142819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854C>T
AA Mutation	p.Ala285Val(p.A285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134143608:134143608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766182177
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134143090:134143090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134138107:134138107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775076567
CDS Mutation	c.490G>A
AA Mutation	p.Glu164Lys(p.E164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134142294:134142294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143237515
CDS Mutation	c.745G>A
AA Mutation	p.Asp249Asn(p.D249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342854
Start	134139015:134139015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342854
Start	134143612:134143612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754914783
CDS Mutation	c.1047G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342854
Start	134138074:134138074(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.463delC
AA Mutation	p.His155ThrfsTer44(p.H155Tfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342854
Start	134138095:134138098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773062085
CDS Mutation	c.484_487delCTCT
AA Mutation	p.Leu162ThrfsTer36(p.L162Tfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342854
Start	134115989:134115989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.402delC
AA Mutation	p.Ser135ArgfsTer64(p.S135Rfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000342854
Start	134138965:134138965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>T
AA Mutation	p.Gln188Ter(p.Q188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342854
Start	134142260:134142261(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.717dupC
AA Mutation	p.Ser240LeufsTer55(p.S240Lfs*55)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TCF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134138107:134138107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775076567
CDS Mutation	c.490G>A
AA Mutation	p.Glu164Lys(p.E164K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342854
Start	134142775:134142775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810G>T
AA Mutation	p.Lys270Asn(p.K270N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript