Colon Cancer: Gene >> RAD52

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358495
Start	913903:913903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112677599
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Cys(p.R396C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358495
Start	927173:927173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439G>A
AA Mutation	p.Val147Met(p.V147M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358495
Start	916771:916771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>T
AA Mutation	p.Pro198Leu(p.P198L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358495
Start	916363:916363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765891551
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358495
Start	916662:916662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000358495
Start	914440:914440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>T
AA Mutation	p.Glu320Ter(p.E320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAD52

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358495
Start	933026:933026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358495
Start	914507:914507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373796726
CDS Mutation	c.891G>A
Mutation Classification	Silent
Feature Type	Transcript