Mutation

Primary Site >> Stomach Cancer

Gene >> PTPRO

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15501797:15501797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201019396
CDS Mutation	c.839C>A
AA Mutation	p.Ser280Tyr(p.S280Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15484073:15484073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175A>G
AA Mutation	p.Lys59Glu(p.K59E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15526197:15526197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099A>C
AA Mutation	p.Asn700Thr(p.N700T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15501839:15501839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779152143
CDS Mutation	c.881C>T
AA Mutation	p.Thr294Met(p.T294M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15516894:15516894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1717A>C
AA Mutation	p.Met573Leu(p.M573L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15578878:15578878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2855T>C
AA Mutation	p.Ile952Thr(p.I952T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15508706:15508706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403T>A
AA Mutation	p.Val468Glu(p.V468E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15516912:15516912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1735A>G
AA Mutation	p.Thr579Ala(p.T579A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15484190:15484190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292G>A
AA Mutation	p.Val98Ile(p.V98I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15497293:15497293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Pro133Leu(p.P133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15581791:15581791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146574957
CDS Mutation	c.3245G>A
AA Mutation	p.Arg1082Gln(p.R1082Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15484019:15484019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141750255
CDS Mutation	c.121G>A
AA Mutation	p.Val41Ile(p.V41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000281171
Start	15497337:15497337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.442A>G
AA Mutation	p.Asn148Asp(p.N148D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15549222:15549222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2433A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281171
Start	15551600:15551600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2487T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000281171
Start	15504015:15504015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1213G>T
AA Mutation	p.Gly405Ter(p.G405*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript