Colon Cancer: Gene >> FH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366560
Start	241513674:241513674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>A
AA Mutation	p.Ala103Thr(p.A103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366560
Start	241508740:241508740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601A>T
AA Mutation	p.Ile201Leu(p.I201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366560
Start	241504197:241504197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755449276
CDS Mutation	c.953A>G
AA Mutation	p.His318Arg(p.H318R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366560
Start	241513622:241513622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359T>A
AA Mutation	p.Ile120Lys(p.I120K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366560
Start	241500522:241500522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772415507
CDS Mutation	c.1305G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366560
Start	241513675:241513675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142283468
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366560
Start	241502524:241502524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366560
Start	241506100:241506100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.807C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366560
Start	241512054:241512054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202061330
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript