Colon Cancer: Gene >> FCGR2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543859
Start	161589712:161589712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187810534
CDS Mutation	c.281C>T
AA Mutation	p.Thr94Met(p.T94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543859
Start	161589752:161589752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543859
Start	161589698:161589698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543859
Start	161599707:161599707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201572445
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543859
Start	161589713:161589713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FCGR2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543859
Start	161589753:161589753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754724878
CDS Mutation	c.322G>A
AA Mutation	p.Gly108Arg(p.G108R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543859
Start	161599761:161599761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript