Mutation

Primary Site >> Stomach Cancer

Gene >> PTPRD

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8486014:8486014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375803455
CDS Mutation	c.2803G>A
AA Mutation	p.Val935Ile(p.V935I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8436611:8436611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4067A>C
AA Mutation	p.Lys1356Thr(p.K1356T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8636729:8636729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180A>C
AA Mutation	p.Lys60Asn(p.K60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356435
Start	8339045:8339045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5256G>T
AA Mutation	p.Glu1752Asp(p.E1752D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8331655:8331655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5461A>G
AA Mutation	p.Ile1821Val(p.I1821V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8485824:8485824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547908736
CDS Mutation	c.2993C>T
AA Mutation	p.Thr998Met(p.T998M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8465548:8465548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3632A>G
AA Mutation	p.Tyr1211Cys(p.Y1211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8504278:8504278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805C>T
AA Mutation	p.Ala602Val(p.A602V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8499822:8499822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758558790
CDS Mutation	c.2147G>A
AA Mutation	p.Arg716His(p.R716H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8485951:8485951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2866C>A
AA Mutation	p.Leu956Ile(p.L956I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8376048:8376048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4549A>C
AA Mutation	p.Thr1517Pro(p.T1517P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8317890:8317890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5723A>G
AA Mutation	p.Asp1908Gly(p.D1908G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8633320:8633320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Trp(p.R117W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356435
Start	8521544:8521544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8341799:8341799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4841C>G
AA Mutation	p.Thr1614Ser(p.T1614S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8341129:8341129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5087G>T
AA Mutation	p.Gly1696Val(p.G1696V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8636748:8636748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>C
AA Mutation	p.Lys54Thr(p.K54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8465495:8465495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3685G>A
AA Mutation	p.Val1229Met(p.V1229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8504266:8504266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817A>G
AA Mutation	p.Gln606Arg(p.Q606R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8521506:8521506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.732T>A
AA Mutation	p.Asn244Lys(p.N244K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8317903:8317903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5710C>G
AA Mutation	p.Leu1904Val(p.L1904V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8486247:8486247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139171396
CDS Mutation	c.2570G>A
AA Mutation	p.Arg857His(p.R857H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8518139:8518139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252T>C
AA Mutation	p.Ser418Pro(p.S418P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8486161:8486161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2656C>G
AA Mutation	p.His886Asp(p.H886D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8465638:8465638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781067774
CDS Mutation	c.3542G>A
AA Mutation	p.Arg1181His(p.R1181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8485893:8485893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2924C>T
AA Mutation	p.Ala975Val(p.A975V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8525005:8525005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599C>T
AA Mutation	p.Ser200Phe(p.S200F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8633359:8633359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Val104Met(p.V104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8484153:8484153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3379C>A
AA Mutation	p.Gln1127Lys(p.Q1127K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8500960:8500960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922T>C
AA Mutation	p.Ile641Thr(p.I641T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8518133:8518133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>A
AA Mutation	p.Ala420Thr(p.A420T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8521543:8521543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Arg232His(p.R232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8518099:8518099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764400127
CDS Mutation	c.1292C>T
AA Mutation	p.Ser431Leu(p.S431L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8518071:8518071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320A>C
AA Mutation	p.Glu440Asp(p.E440D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000356435
Start	8485953:8485953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2864C>A
AA Mutation	p.Thr955Asn(p.T955N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8518269:8518269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137892356
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8389280:8389280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4338A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8340388:8340388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5208T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8517924:8517924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8518230:8518230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779673772
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8449774:8449774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3939C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8521488:8521488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147417729
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8404618:8404618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4129T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8499815:8499815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752774320
CDS Mutation	c.2154C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8521482:8521482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765489687
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8486162:8486162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754293267
CDS Mutation	c.2655C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8486270:8486270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2547A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8500770:8500770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356435
Start	8636819:8636819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356435
Start	8518185:8518185(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1206delG
AA Mutation	p.Pro403LeufsTer7(p.P403Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000356435
Start	8460412:8460412(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3874delA
AA Mutation	p.Arg1292GlyfsTer28(p.R1292Gfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	stop_gained
Transcription ID	ENST00000356435
Start	8341911:8341911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4729A>T
AA Mutation	p.Lys1577Ter(p.K1577*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	53
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356435
Start	8449838:8449838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3876-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript