Colon Cancer: Gene >> FCGR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369168
Start	149788474:149788474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374578876
CDS Mutation	c.416G>A
AA Mutation	p.Arg139Gln(p.R139Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369168
Start	149791426:149791426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Arg345Lys(p.R345K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369168
Start	149790204:149790204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782812046
CDS Mutation	c.710G>A
AA Mutation	p.Arg237Gln(p.R237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369168
Start	149791514:149791514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587640055
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369168
Start	149784037:149784037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369168
Start	149790202:149790202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369168
Start	149788473:149788473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FCGR1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369168
Start	149791354:149791354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.962A>C
AA Mutation	p.Lys321Thr(p.K321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369168
Start	149790211:149790211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript