Colon Cancer: Gene >> APEX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457213:20457213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778698391
CDS Mutation	c.662G>A
AA Mutation	p.Arg221His(p.R221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457364:20457364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813G>T
AA Mutation	p.Met271Ile(p.M271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457240:20457240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689C>A
AA Mutation	p.Ala230Asp(p.A230D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20456810:20456810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Asp(p.G130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457239:20457239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Ala230Thr(p.A230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> APEX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457128:20457128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778301776
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Cys(p.R193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216714
Start	20457372:20457372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374977590
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript