Colon Cancer: Gene >> PEX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7203486:7203486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767306549
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Trp(p.R301W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7209764:7209764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1642G>A
AA Mutation	p.Ala548Thr(p.A548T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7209770:7209770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>A
AA Mutation	p.Glu550Lys(p.E550K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7209798:7209798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676G>A
AA Mutation	p.Arg559His(p.R559H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7208077:7208077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145690714
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7207783:7207783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091A>G
AA Mutation	p.Gln364Arg(p.Q364R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420616
Start	7210196:7210196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143610074
CDS Mutation	c.1893C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420616
Start	7199105:7199105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138205085
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420616
Start	7208075:7208075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000420616
Start	7202684:7202684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267608194
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Ter(p.R276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PEX5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7208488:7208488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>T
AA Mutation	p.Ala405Ser(p.A405S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420616
Start	7203441:7203441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.856G>A
AA Mutation	p.Asp286Asn(p.D286N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420616
Start	7191252:7191252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript