Colon Cancer: Gene >> FCGR3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367967
Start	161544935:161544935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778260076
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Trp(p.R115W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367967
Start	161544907:161544907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371T>G
AA Mutation	p.Ile124Ser(p.I124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367967
Start	161549017:161549017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370288605
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Trp(p.R19W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367967
Start	161543076:161543076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573034150
CDS Mutation	c.701G>A
AA Mutation	p.Arg234Gln(p.R234Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367967
Start	161543123:161543123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FCGR3A

No Mutation Annotation!