Colon Cancer: Gene >> PTPRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15497307:15497307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>A
AA Mutation	p.Leu138Met(p.L138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15565600:15565600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2719A>C
AA Mutation	p.Asn907His(p.N907H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15504062:15504062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260T>G
AA Mutation	p.Phe420Leu(p.F420L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15524838:15524838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1916C>A
AA Mutation	p.Ser639Tyr(p.S639Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15524826:15524826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1904C>T
AA Mutation	p.Pro635Leu(p.P635L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15589462:15589462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3418G>A
AA Mutation	p.Val1140Met(p.V1140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15551593:15551593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2480C>T
AA Mutation	p.Ala827Val(p.A827V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15578857:15578857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2834T>G
AA Mutation	p.Leu945Trp(p.L945W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15499490:15499490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557G>T
AA Mutation	p.Cys186Phe(p.C186F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15551585:15551585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752317809
CDS Mutation	c.2472C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15501654:15501654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764927770
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15569435:15569435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186385650
CDS Mutation	c.2766C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15484027:15484027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15484018:15484018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000281171
Start	15565624:15565627(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2744_2747delCAAA
AA Mutation	p.Asn916ArgfsTer29(p.N916Rfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000281171
Start	15508661:15508661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358G>A
AA Mutation	p.Trp453Ter(p.W453*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000281171
Start	15581754:15581754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3208G>T
AA Mutation	p.Glu1070Ter(p.E1070*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PTPRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15508681:15508681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378T>G
AA Mutation	p.Tyr460Asp(p.Y460D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15484042:15484042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144C>A
AA Mutation	p.Asp48Glu(p.D48E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15549179:15549179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390G>A
AA Mutation	p.Ser797Asn(p.S797N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15557495:15557495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2599G>A
AA Mutation	p.Glu867Lys(p.E867K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15484102:15484102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>A
AA Mutation	p.Phe68Leu(p.F68L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15484102:15484102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15501966:15501966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript