Colon Cancer: Gene >> TFCP2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263707
Start	121242457:121242457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765369796
CDS Mutation	c.670G>A
AA Mutation	p.Asp224Asn(p.D224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263707
Start	121237627:121237627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263707
Start	121249043:121249043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150968715
CDS Mutation	c.336G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263707
Start	121231961:121231961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145068402
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263707
Start	121231888:121231888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1279delC
AA Mutation	p.Gln427SerfsTer18(p.Q427Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TFCP2L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263707
Start	121231833:121231833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768235839
CDS Mutation	c.1334G>A
AA Mutation	p.Ser445Asn(p.S445N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000263707
Start	121246907:121246907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Ter(p.R190*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript