Colon Cancer: Gene >> FFAR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371483
Start	93587386:93587386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911T>C
AA Mutation	p.Leu304Pro(p.L304P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371483
Start	93587476:93587476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001C>A
AA Mutation	p.Pro334His(p.P334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371483
Start	93579180:93579180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371483
Start	93587581:93587581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106G>T
AA Mutation	p.Arg369Ile(p.R369I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371483
Start	93587423:93587423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113451789
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FFAR4

No Mutation Annotation!