Colon Cancer: Gene >> FCGR2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271450
Start	161509960:161509960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>A
AA Mutation	p.Asp169Asn(p.D169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271450
Start	161506424:161506424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750989159
CDS Mutation	c.197G>A
AA Mutation	p.Arg66His(p.R66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000271450
Start	161513894:161513894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FCGR2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271450
Start	161506448:161506448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773080023
CDS Mutation	c.221A>C
AA Mutation	p.Gln74Pro(p.Q74P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271450
Start	161510037:161510037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79273228
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271450
Start	161518052:161518052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145803059
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript