Colon Cancer: Gene >> PTPRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70660964:70660964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144147611
CDS Mutation	c.1742G>A
AA Mutation	p.Arg581Gln(p.R581Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70662511:70662511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1592G>A
AA Mutation	p.Arg531Gln(p.R531Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70698285:70698285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752997522
CDS Mutation	c.1259G>A
AA Mutation	p.Arg420His(p.R420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70684742:70684742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192322137
CDS Mutation	c.1321G>A
AA Mutation	p.Asp441Asn(p.D441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70684138:70684138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1486G>C
AA Mutation	p.Glu496Gln(p.E496Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70745918:70745918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370625173
CDS Mutation	c.907G>A
AA Mutation	p.Val303Met(p.V303M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70754213:70754213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765894494
CDS Mutation	c.716T>G
AA Mutation	p.Val239Gly(p.V239G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70701210:70701210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121C>T
AA Mutation	p.Ala374Val(p.A374V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283228
Start	70892916:70892916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367712274
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283228
Start	70761517:70761517(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.581delT
AA Mutation	p.Leu194CysfsTer48(p.L194Cfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283228
Start	70684131:70684131(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1493delA
AA Mutation	p.Asn498MetfsTer25(p.N498Mfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000283228
Start	70745903:70745903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Ter(p.R308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000283228
Start	70662493:70662493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70761539:70761539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Cys(p.R187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70656714:70656714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870C>T
AA Mutation	p.Arg624Cys(p.R624C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283228
Start	70698288:70698288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256A>C
AA Mutation	p.Asn419Thr(p.N419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000283228
Start	70662512:70662512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760678361
CDS Mutation	c.1591C>T
AA Mutation	p.Arg531Ter(p.R531*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000283228
Start	70684138:70684138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1486G>T
AA Mutation	p.Glu496Ter(p.E496*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript