Colon Cancer: Gene >> FCAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355524
Start	54885492:54885492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143972917
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Trp(p.R110W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355524
Start	54888120:54888120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>T
AA Mutation	p.Ala159Ser(p.A159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355524
Start	54888171:54888171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355524
Start	54888282:54888282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756874719
CDS Mutation	c.637C>T
AA Mutation	p.Leu213Phe(p.L213F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355524
Start	54885419:54885419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000355524
Start	54885332:54885332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>A
AA Mutation	p.Tyr56Ter(p.Y56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FCAR

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355524
Start	54889695:54889695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769864643
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000355524
Start	54885369:54885369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766003893
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Ter(p.R69*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript