Mutation

Primary Site >> Stomach Cancer

Gene >> VCAN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538131:83538131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5128G>A
AA Mutation	p.Asp1710Asn(p.D1710N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83537394:83537394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4391C>G
AA Mutation	p.Ala1464Gly(p.A1464G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538891:83538891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5888C>T
AA Mutation	p.Ala1963Val(p.A1963V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540428:83540428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7425A>C
AA Mutation	p.Lys2475Asn(p.K2475N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83580350:83580350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10107T>A
AA Mutation	p.Asn3369Lys(p.N3369K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83541299:83541299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752544304
CDS Mutation	c.8296T>C
AA Mutation	p.Ser2766Pro(p.S2766P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83520839:83520839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2533A>C
AA Mutation	p.Ser845Arg(p.S845R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540052:83540052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7049C>G
AA Mutation	p.Pro2350Arg(p.P2350R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83541096:83541096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770058352
CDS Mutation	c.8093A>C
AA Mutation	p.Lys2698Thr(p.K2698T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83522232:83522232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149651541
CDS Mutation	c.3926C>T
AA Mutation	p.Thr1309Met(p.T1309M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83541986:83541986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8983A>C
AA Mutation	p.Ser2995Arg(p.S2995R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83519369:83519369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143128206
CDS Mutation	c.1063G>A
AA Mutation	p.Asp355Asn(p.D355N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83537904:83537904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765791345
CDS Mutation	c.4901C>A
AA Mutation	p.Ser1634Tyr(p.S1634Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538821:83538821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5818G>A
AA Mutation	p.Glu1940Lys(p.E1940K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83539101:83539101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6098T>G
AA Mutation	p.Phe2033Cys(p.F2033C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83519425:83519425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749460528
CDS Mutation	c.1119G>A
AA Mutation	p.Met373Ile(p.M373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538040:83538040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5037A>C
AA Mutation	p.Glu1679Asp(p.E1679D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540940:83540940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7937A>G
AA Mutation	p.Tyr2646Cys(p.Y2646C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83580024:83580024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9925G>A
AA Mutation	p.Gly3309Arg(p.G3309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540061:83540061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200015194
CDS Mutation	c.7058C>T
AA Mutation	p.Thr2353Met(p.T2353M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83537097:83537097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773919986
CDS Mutation	c.4094A>G
AA Mutation	p.His1365Arg(p.H1365R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540368:83540368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7365C>A
AA Mutation	p.Ser2455Arg(p.S2455R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540585:83540585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772985425
CDS Mutation	c.7582G>A
AA Mutation	p.Glu2528Lys(p.E2528K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538243:83538243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376380721
CDS Mutation	c.5240C>T
AA Mutation	p.Ser1747Leu(p.S1747L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540118:83540118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7115G>T
AA Mutation	p.Ser2372Ile(p.S2372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83541600:83541600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8597A>T
AA Mutation	p.Lys2866Met(p.K2866M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83520567:83520567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2261C>A
AA Mutation	p.Thr754Lys(p.T754K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83520446:83520446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2140G>A
AA Mutation	p.Gly714Arg(p.G714R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83519574:83519574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268T>C
AA Mutation	p.Leu423Ser(p.L423S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83537787:83537787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4784T>G
AA Mutation	p.Val1595Gly(p.V1595G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83519684:83519684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.Leu460Phe(p.L460F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83512337:83512337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983T>A
AA Mutation	p.Phe328Tyr(p.F328Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83519384:83519384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374992475
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83580420:83580420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10177G>C
AA Mutation	p.Glu3393Gln(p.E3393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83540489:83540489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7486A>G
AA Mutation	p.Asn2496Asp(p.N2496D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83521978:83521978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3672G>T
AA Mutation	p.Lys1224Asn(p.K1224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83539661:83539661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6658C>T
AA Mutation	p.His2220Tyr(p.H2220Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83580424:83580424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532877615
CDS Mutation	c.10181C>T
AA Mutation	p.Ser3394Leu(p.S3394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83538621:83538621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767479742
CDS Mutation	c.5618A>G
AA Mutation	p.His1873Arg(p.H1873R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83580347:83580347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10104A>C
AA Mutation	p.Lys3368Asn(p.K3368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000265077
Start	83520839:83520839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2533A>G
AA Mutation	p.Ser845Gly(p.S845G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83538601:83538601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5598A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83540273:83540273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7270T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83540971:83540971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7968T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83579987:83579987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758458805
CDS Mutation	c.9888C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83519701:83519701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772684866
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83493897:83493897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83541955:83541955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8952T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83520283:83520283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83541865:83541865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8862T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83520598:83520598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2292A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83520148:83520148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83545562:83545562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375652154
CDS Mutation	c.9291G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83555035:83555035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9732A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83521201:83521201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141161041
CDS Mutation	c.2895T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83521282:83521282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2976A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83538955:83538955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5952T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	58
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83519470:83519470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	59
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83538304:83538304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5301A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	60
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83540419:83540419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7416A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	61
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83521642:83521642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3336C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	62
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83537029:83537029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4026A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	63
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83539621:83539621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6618C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	64
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265077
Start	83539714:83539714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747734140
CDS Mutation	c.6711G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	65
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265077
Start	83520238:83520238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1935delT
AA Mutation	p.Pro646HisfsTer8(p.P646Hfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	66
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265077
Start	83537549:83537549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4551delA
AA Mutation	p.Ala1519GlnfsTer42(p.A1519Qfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	67
Mutation Consequence	stop_gained
Transcription ID	ENST00000265077
Start	83483554:83483554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36T>A
AA Mutation	p.Cys12Ter(p.C12*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	68
Mutation Consequence	stop_gained
Transcription ID	ENST00000265077
Start	83539772:83539772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6769G>T
AA Mutation	p.Gly2257Ter(p.G2257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	69
Mutation Consequence	stop_gained
Transcription ID	ENST00000265077
Start	83540765:83540765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7762G>T
AA Mutation	p.Glu2588Ter(p.E2588*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	70
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265077
Start	83539975:83539976(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6975dupG
AA Mutation	p.Ser2326ValfsTer13(p.S2326Vfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	71
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265077
Start	83554955:83554955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9653-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript