Mutation

Primary Site >> Stomach Cancer

Gene >> ACAN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88857293:88857293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4708C>T
AA Mutation	p.Pro1570Ser(p.P1570S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88845805:88845805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1352G>A
AA Mutation	p.Gly451Asp(p.G451D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88847952:88847952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1646A>C
AA Mutation	p.Lys549Thr(p.K549T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88871388:88871388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6953A>T
AA Mutation	p.Glu2318Val(p.E2318V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88849578:88849578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1873G>A
AA Mutation	p.Gly625Ser(p.G625S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88858979:88858979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6394A>C
AA Mutation	p.Thr2132Pro(p.T2132P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88857807:88857807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5222G>T
AA Mutation	p.Gly1741Val(p.G1741V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88838938:88838938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760009352
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88857330:88857330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763243954
CDS Mutation	c.4745G>A
AA Mutation	p.Gly1582Glu(p.G1582E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88859072:88859072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766547434
CDS Mutation	c.6487G>A
AA Mutation	p.Ala2163Thr(p.A2163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88849614:88849614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770581471
CDS Mutation	c.1909G>A
AA Mutation	p.Val637Ile(p.V637I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88857941:88857941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5356A>C
AA Mutation	p.Ser1786Arg(p.S1786R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88838963:88838963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757439227
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88840128:88840128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527447898
CDS Mutation	c.571G>A
AA Mutation	p.Ala191Thr(p.A191T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88847942:88847942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62640041
CDS Mutation	c.1636G>A
AA Mutation	p.Val546Met(p.V546M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88854940:88854940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2355G>T
AA Mutation	p.Glu785Asp(p.E785D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88873988:88873988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746885216
CDS Mutation	c.7480G>A
AA Mutation	p.Gly2494Arg(p.G2494R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88839037:88839037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>A
AA Mutation	p.Val149Met(p.V149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88873926:88873926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7418G>T
AA Mutation	p.Arg2473Leu(p.R2473L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88838869:88838869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565318742
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Cys(p.R93C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88855148:88855148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2563C>T
AA Mutation	p.Pro855Ser(p.P855S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88849639:88849639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750579987
CDS Mutation	c.1934G>T
AA Mutation	p.Gly645Val(p.G645V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88858277:88858277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761003367
CDS Mutation	c.5692C>T
AA Mutation	p.Pro1898Ser(p.P1898S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88872896:88872896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751606366
CDS Mutation	c.7204C>T
AA Mutation	p.Arg2402Cys(p.R2402C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000439576
Start	88843415:88843415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818G>A
AA Mutation	p.Cys273Tyr(p.C273Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88841767:88841767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88855240:88855240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2655G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88860387:88860387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373512626
CDS Mutation	c.6894A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88841767:88841767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88860432:88860432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6939T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439576
Start	88847962:88847962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1656C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439576
Start	88855121:88855121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2541delC
AA Mutation	p.Val848CysfsTer97(p.V848Cfs*97)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000439576
Start	88855021:88855021(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2439delC
AA Mutation	p.Ser814GlnfsTer131(p.S814Qfs*131)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript