Colon Cancer: Gene >> PTPRJ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48128017:48128017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761076895
CDS Mutation	c.1331C>T
AA Mutation	p.Thr444Met(p.T444M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48121245:48121245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595A>G
AA Mutation	p.Arg199Gly(p.R199G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48145049:48145049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2836G>A
AA Mutation	p.Gly946Arg(p.G946R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48125009:48125009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916G>A
AA Mutation	p.Ala306Thr(p.A306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48112926:48112926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295C>T
AA Mutation	p.Pro99Ser(p.P99S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48136111:48136111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767845396
CDS Mutation	c.1688C>T
AA Mutation	p.Pro563Leu(p.P563L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48136074:48136074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769547786
CDS Mutation	c.1651G>A
AA Mutation	p.Val551Ile(p.V551I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48139759:48139759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2426G>A
AA Mutation	p.Cys809Tyr(p.C809Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123757:48123757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148218497
CDS Mutation	c.761G>T
AA Mutation	p.Arg254Ile(p.R254I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48156054:48156054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536396969
CDS Mutation	c.3373C>T
AA Mutation	p.Arg1125Cys(p.R1125C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48130650:48130650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549T>C
AA Mutation	p.Phe517Leu(p.F517L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48160025:48160025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3534C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48155865:48155865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48136217:48136217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369760760
CDS Mutation	c.1794G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48167245:48167245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3897C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48121073:48121073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48146892:48146892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752139572
CDS Mutation	c.2928G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48137124:48137124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1995A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48136073:48136073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148782546
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48139619:48139619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751724128
CDS Mutation	c.2286G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRJ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48121144:48121144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494T>C
AA Mutation	p.Val165Ala(p.V165A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123837:48123837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841A>C
AA Mutation	p.Lys281Gln(p.K281Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000418331
Start	48150181:48150181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765457377
CDS Mutation	c.3136G>A
AA Mutation	p.Glu1046Lys(p.E1046K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48150117:48150117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3072G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48139619:48139619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751724128
CDS Mutation	c.2286G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48156032:48156032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3351G>A
Mutation Classification	Silent
Feature Type	Transcript