Colon Cancer: Gene >> FGR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374003
Start	27613017:27613017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141451773
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374003
Start	27615482:27615482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142690351
CDS Mutation	c.970G>A
AA Mutation	p.Val324Met(p.V324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374003
Start	27623886:27623886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31C>T
AA Mutation	p.Pro11Ser(p.P11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374003
Start	27616963:27616963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779867650
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374003
Start	27623884:27623884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148928565
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGR

No Mutation Annotation!