Colon Cancer: Gene >> PTPRE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128082846:128082846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2043C>A
AA Mutation	p.Phe681Leu(p.F681L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128070421:128070421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764490854
CDS Mutation	c.1264G>A
AA Mutation	p.Asp422Asn(p.D422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128047793:128047793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239G>A
AA Mutation	p.Ser80Asn(p.S80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128040934:128040934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53G>T
AA Mutation	p.Arg18Met(p.R18M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128068211:128068211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932T>C
AA Mutation	p.Ile311Thr(p.I311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128070848:128070848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762233896
CDS Mutation	c.1334C>T
AA Mutation	p.Thr445Met(p.T445M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128077671:128077671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745941150
CDS Mutation	c.1780G>A
AA Mutation	p.Gly594Ser(p.G594S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128061702:128061702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612C>A
AA Mutation	p.Phe204Leu(p.F204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128066099:128066099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>A
AA Mutation	p.Asp250Asn(p.D250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128069805:128069805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128066161:128066161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128070861:128070861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773837527
CDS Mutation	c.1347G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128069728:128069728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779391135
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128068245:128068245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370133452
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128068254:128068254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200495195
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128068134:128068134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201293516
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254667
Start	128070823:128070823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777749200
CDS Mutation	c.1309C>T
AA Mutation	p.Arg437Trp(p.R437W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128070366:128070366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140843679
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128082846:128082846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2043C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254667
Start	128070420:128070420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141078040
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript