Mutation

Primary Site >> Stomach Cancer

Gene >> PTPRJ

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48112824:48112824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193G>A
AA Mutation	p.Ala65Thr(p.A65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48144716:48144716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755218393
CDS Mutation	c.2617G>A
AA Mutation	p.Asp873Asn(p.D873N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
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

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48145109:48145109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2896T>G
AA Mutation	p.Leu966Val(p.L966V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48150113:48150113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3068T>C
AA Mutation	p.Val1023Ala(p.V1023A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48167319:48167319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199803858
CDS Mutation	c.3971C>T
AA Mutation	p.Ala1324Val(p.A1324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48155822:48155822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3251T>G
AA Mutation	p.Leu1084Arg(p.L1084R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48110067:48110067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Ala36Thr(p.A36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48125013:48125013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>A
AA Mutation	p.Pro307His(p.P307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48163614:48163614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3715T>C
AA Mutation	p.Cys1239Arg(p.C1239R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48139561:48139561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2228C>A
AA Mutation	p.Pro743His(p.P743H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
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

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48156055:48156055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374260795
CDS Mutation	c.3374G>A
AA Mutation	p.Arg1125His(p.R1125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123621:48123621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625C>A
AA Mutation	p.Pro209Thr(p.P209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48136182:48136182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759T>C
AA Mutation	p.Tyr587His(p.Y587H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48137128:48137128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1999T>C
AA Mutation	p.Ser667Pro(p.S667P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48137030:48137030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1901T>C
AA Mutation	p.Val634Ala(p.V634A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123625:48123625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>C
AA Mutation	p.Val210Ala(p.V210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123696:48123696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>A
AA Mutation	p.Ala234Thr(p.A234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48130504:48130504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140690947
CDS Mutation	c.1403C>T
AA Mutation	p.Thr468Met(p.T468M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000418331
Start	48123730:48123730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753741250
CDS Mutation	c.734G>A
AA Mutation	p.Ser245Asn(p.S245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48127799:48127799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780863107
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48130496:48130496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48145081:48145081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2868C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48167350:48167350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4002T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48144820:48144820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532049445
CDS Mutation	c.2721C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418331
Start	48127865:48127865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748897376
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418331
Start	48139741:48139741(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2412delC
AA Mutation	p.Thr805ProfsTer29(p.T805Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418331
Start	48127898:48127898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1216delG
AA Mutation	p.Glu406ArgfsTer33(p.E406Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418331
Start	48136264:48136264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1846delG
AA Mutation	p.Asp616ThrfsTer19(p.D616Tfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000418331
Start	48155800:48155800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3230-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	32
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000418331
Start	48150095:48150095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3051-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript