Colon Cancer: Gene >> RRM2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000304567
Start	10123737:10123737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320T>C
AA Mutation	p.Val107Ala(p.V107A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304567
Start	10124783:10124783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502A>G
AA Mutation	p.Met168Val(p.M168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304567
Start	10128862:10128862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813T>G
AA Mutation	p.Asp271Glu(p.D271E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304567
Start	10123403:10123403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.195delC
AA Mutation	p.Gly66AlafsTer8(p.G66Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000304567
Start	10129156:10129156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1017+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RRM2

No Mutation Annotation!