Colon Cancer: Gene >> FFAR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246553
Start	35352171:35352171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620G>A
AA Mutation	p.Arg207Gln(p.R207Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246553
Start	35352323:35352323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772C>T
AA Mutation	p.Arg258Trp(p.R258W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246553
Start	35351862:35351862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753588393
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246553
Start	35352160:35352160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246553
Start	35352079:35352079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777875100
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246553
Start	35351827:35351827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FFAR1

No Mutation Annotation!