Colon Cancer: Gene >> F2RL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296677
Start	76833033:76833033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296677
Start	76833537:76833537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296677
Start	76833690:76833690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745368730
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296677
Start	76833678:76833678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754604267
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000296677
Start	76833415:76833415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369747168
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Ter(p.R270*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> F2RL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296677
Start	76832915:76832915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185549069
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296677
Start	76833625:76833625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018G>A
AA Mutation	p.Asp340Asn(p.D340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296677
Start	76833126:76833126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript