Mutation

Primary Site >> Stomach Cancer

Gene >> PTPRB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70562991:70562991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3367G>A
AA Mutation	p.Asp1123Asn(p.D1123N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261266
Start	70534835:70534835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374775162
CDS Mutation	c.5548G>A
AA Mutation	p.Gly1850Ser(p.G1850S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70524566:70524566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5876G>A
AA Mutation	p.Cys1959Tyr(p.C1959Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70555192:70555192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4457A>T
AA Mutation	p.Lys1486Ile(p.K1486I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70569686:70569686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763439556
CDS Mutation	c.2969T>C
AA Mutation	p.Val990Ala(p.V990A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334414
Start	70622390:70622390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>C
AA Mutation	p.Glu236Asp(p.E236D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70592353:70592353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768944578
CDS Mutation	c.1055G>A
AA Mutation	p.Arg352Gln(p.R352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70609119:70609119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275A>C
AA Mutation	p.Asn92Thr(p.N92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70524522:70524522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750940787
CDS Mutation	c.5920G>C
AA Mutation	p.Glu1974Gln(p.E1974Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70555887:70555887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4322C>A
AA Mutation	p.Thr1441Asn(p.T1441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70581135:70581135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1825A>T
AA Mutation	p.Ser609Cys(p.S609C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70563039:70563039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200923003
CDS Mutation	c.3319G>A
AA Mutation	p.Ala1107Thr(p.A1107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70609212:70609212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182A>G
AA Mutation	p.Asp61Gly(p.D61G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70569740:70569740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2915A>G
AA Mutation	p.Tyr972Cys(p.Y972C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70562879:70562879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3479A>T
AA Mutation	p.Glu1160Val(p.E1160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70566503:70566503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3182A>T
AA Mutation	p.Tyr1061Phe(p.Y1061F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70569891:70569891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2764G>T
AA Mutation	p.Asp922Tyr(p.D922Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70539830:70539830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5039C>T
AA Mutation	p.Ser1680Phe(p.S1680F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261266
Start	70571097:70571097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760734939
CDS Mutation	c.2645G>A
AA Mutation	p.Arg882His(p.R882H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70571135:70571135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758474846
CDS Mutation	c.2607C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70532062:70532062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5823T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70555212:70555212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112766507
CDS Mutation	c.4437C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70581190:70581190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70560735:70560735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111361328
CDS Mutation	c.3714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261266
Start	70552908:70552908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192182815
CDS Mutation	c.4602C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70555303:70555303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4346delC
AA Mutation	p.Pro1449LeufsTer9(p.P1449Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70596184:70596184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.469delG
AA Mutation	p.Val157PhefsTer50(p.V157Ffs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261266
Start	70594587:70594587(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.742delG
AA Mutation	p.Val248TrpfsTer13(p.V248Wfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261266
Start	70566706:70566706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2981-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261266
Start	70609067:70609067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript