Colon Cancer: Gene >> OGG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344629
Start	9751810:9751810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426C>A
AA Mutation	p.Phe142Leu(p.F142L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302036
Start	9765945:9765945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085G>A
AA Mutation	p.Ser362Asn(p.S362N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344629
Start	9751800:9751800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416A>G
AA Mutation	p.Glu139Gly(p.E139G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344629
Start	9756577:9756577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750447639
CDS Mutation	c.854C>T
AA Mutation	p.Thr285Met(p.T285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344629
Start	9754871:9754871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733G>A
AA Mutation	p.Gly245Arg(p.G245R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344629
Start	9751867:9751867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OGG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344629
Start	9757076:9757076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>T
AA Mutation	p.Asp322Tyr(p.D322Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344629
Start	9751798:9751798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745763093
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript