Colon Cancer: Gene >> TFCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257915
Start	51172389:51172389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34G>A
AA Mutation	p.Glu12Lys(p.E12K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257915
Start	51117729:51117729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769638214
CDS Mutation	c.293G>A
AA Mutation	p.Arg98Gln(p.R98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257915
Start	51103714:51103714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563834540
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	ENST00000257915
Start	51099730:51099730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201T>A
AA Mutation	p.Leu401Met(p.L401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257915
Start	51109175:51109175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763123343
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257915
Start	51098864:51098865(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1330dupA
AA Mutation	p.Ile444AsnfsTer29(p.I444Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000257915
Start	51117748:51117748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TFCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257915
Start	51103714:51103714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563834540
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript