Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4138258:4138258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2254C>G
AA Mutation	p.Leu752Val(p.L752V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4127060:4127060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496G>A
AA Mutation	p.Arg499His(p.R499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4106190:4106190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253A>G
AA Mutation	p.Asn85Asp(p.N85D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4138222:4138222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218A>T
AA Mutation	p.Arg740Trp(p.R740W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4121706:4121706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979G>T
AA Mutation	p.Asp327Tyr(p.D327Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4135260:4135260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2180G>A
AA Mutation	p.Gly727Asp(p.G727D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300738
Start	4121720:4121720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750572935
CDS Mutation	c.993T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RRM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4118424:4118424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755T>A
AA Mutation	p.Val252Glu(p.V252E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300738
Start	4127060:4127060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496G>A
AA Mutation	p.Arg499His(p.R499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript