Mutation

Primary Site >> Stomach Cancer

Gene >> HSPG2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21884567:21884567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1615C>A
AA Mutation	p.Gln539Lys(p.Q539K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21848774:21848774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7606G>C
AA Mutation	p.Val2536Leu(p.V2536L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21842781:21842781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143274889
CDS Mutation	c.8899G>A
AA Mutation	p.Ala2967Thr(p.A2967T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21833590:21833590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10855A>G
AA Mutation	p.Ser3619Gly(p.S3619G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21875916:21875916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3130G>A
AA Mutation	p.Ala1044Thr(p.A1044T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21861836:21861836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4876C>A
AA Mutation	p.Arg1626Ser(p.R1626S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21865805:21865805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746918802
CDS Mutation	c.4226C>T
AA Mutation	p.Ala1409Val(p.A1409V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21829451:21829451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11924C>A
AA Mutation	p.Pro3975His(p.P3975H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21850085:21850085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7402G>A
AA Mutation	p.Val2468Ile(p.V2468I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21880148:21880148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2302G>T
AA Mutation	p.Gly768Cys(p.G768C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21852984:21852984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6526C>T
AA Mutation	p.Pro2176Ser(p.P2176S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21839031:21839031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762381842
CDS Mutation	c.9944C>T
AA Mutation	p.Thr3315Met(p.T3315M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21839837:21839837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767115080
CDS Mutation	c.9694C>T
AA Mutation	p.Arg3232Cys(p.R3232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374695
Start	21851791:21851791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7006C>A
AA Mutation	p.Pro2336Thr(p.P2336T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21855441:21855441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561814891
CDS Mutation	c.5860G>A
AA Mutation	p.Gly1954Ser(p.G1954S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21828408:21828408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146179360
CDS Mutation	c.12256C>T
AA Mutation	p.Arg4086Trp(p.R4086W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21852138:21852138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190391786
CDS Mutation	c.6820G>A
AA Mutation	p.Ala2274Thr(p.A2274T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21846459:21846459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8305A>G
AA Mutation	p.Ser2769Gly(p.S2769G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21831656:21831656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11348C>T
AA Mutation	p.Ser3783Phe(p.S3783F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21859928:21859928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754726732
CDS Mutation	c.5089C>T
AA Mutation	p.Arg1697Trp(p.R1697W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21854673:21854673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6226G>A
AA Mutation	p.Gly2076Arg(p.G2076R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21828336:21828336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766333633
CDS Mutation	c.12328C>T
AA Mutation	p.Arg4110Cys(p.R4110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21833373:21833373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10990C>T
AA Mutation	p.Pro3664Ser(p.P3664S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21830997:21830997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11656C>A
AA Mutation	p.Leu3886Met(p.L3886M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21851863:21851863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139721678
CDS Mutation	c.6934C>T
AA Mutation	p.Arg2312Trp(p.R2312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21831286:21831286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756266826
CDS Mutation	c.11491G>A
AA Mutation	p.Val3831Ile(p.V3831I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21887507:21887507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148693072
CDS Mutation	c.871G>A
AA Mutation	p.Ala291Thr(p.A291T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21896234:21896234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751202082
CDS Mutation	c.140G>A
AA Mutation	p.Arg47His(p.R47H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21889992:21889992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145847147
CDS Mutation	c.563G>A
AA Mutation	p.Arg188His(p.R188H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21833518:21833518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201309996
CDS Mutation	c.10927G>A
AA Mutation	p.Ala3643Thr(p.A3643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21839992:21839992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748710241
CDS Mutation	c.9539C>T
AA Mutation	p.Ala3180Val(p.A3180V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21884565:21884565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617G>C
AA Mutation	p.Gln539His(p.Q539H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21861993:21861993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4863G>T
AA Mutation	p.Glu1621Asp(p.E1621D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000374695
Start	21843366:21843366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192525833
CDS Mutation	c.8689G>A
AA Mutation	p.Gly2897Arg(p.G2897R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21879059:21879059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770590518
CDS Mutation	c.2406C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21862083:21862083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764396560
CDS Mutation	c.4773C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21890459:21890459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761552629
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21842099:21842099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749580877
CDS Mutation	c.9096C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21844220:21844220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369778477
CDS Mutation	c.8544C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21857157:21857157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140134749
CDS Mutation	c.5433C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21833555:21833555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765627728
CDS Mutation	c.10890A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21834935:21834935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139359384
CDS Mutation	c.10464G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21841203:21841203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533824462
CDS Mutation	c.9411C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21896233:21896233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367794550
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21823638:21823638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147161785
CDS Mutation	c.12981C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21846520:21846520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377526585
CDS Mutation	c.8244C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21851870:21851870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552716935
CDS Mutation	c.6927C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21847761:21847761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371541589
CDS Mutation	c.7953C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21855424:21855424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763580487
CDS Mutation	c.5877A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21823713:21823713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12906C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21876638:21876638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21838841:21838841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10134C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21828046:21828046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12516C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21823692:21823692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369664034
CDS Mutation	c.12927C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21851609:21851609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747613348
CDS Mutation	c.7095C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21853012:21853012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6498G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374695
Start	21851885:21851885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755251798
CDS Mutation	c.6912C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374695
Start	21850176:21850176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7311delC
AA Mutation	p.Thr2438ArgfsTer19(p.T2438Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374695
Start	21872721:21872721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3928delC
AA Mutation	p.His1310ThrfsTer5(p.H1310Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374695
Start	21885149:21885149(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1219delC
AA Mutation	p.Gln407ArgfsTer3(p.Q407Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	61
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374695
Start	21829462:21829462(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.11913delG
AA Mutation	p.Lys3972ArgfsTer58(p.K3972Rfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	62
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374695
Start	21896299:21896299(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.75delG
AA Mutation	p.Leu26Ter(p.L26*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	63
Mutation Consequence	stop_gained
Transcription ID	ENST00000374695
Start	21889996:21889996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Ter(p.R187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	64
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000374695
Start	21839551:21839551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9710-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript