Mutation

Primary Site >> Stomach Cancer

Gene >> ASPM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197143095:197143095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157C>T
AA Mutation	p.Ser386Leu(p.S386L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100607:197100607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201732387
CDS Mutation	c.8644T>C
AA Mutation	p.Tyr2882His(p.Y2882H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197122493:197122493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3493A>G
AA Mutation	p.Thr1165Ala(p.T1165A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197124199:197124199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3301A>G
AA Mutation	p.Arg1101Gly(p.R1101G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197103325:197103325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5926A>T
AA Mutation	p.Ile1976Phe(p.I1976F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197102577:197102577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6674C>A
AA Mutation	p.Ala2225Glu(p.A2225E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197091935:197091935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9416A>G
AA Mutation	p.Lys3139Arg(p.K3139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100819:197100819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8432A>G
AA Mutation	p.Tyr2811Cys(p.Y2811C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100980:197100980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8271A>T
AA Mutation	p.Lys2757Asn(p.K2757N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197122177:197122177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3723T>G
AA Mutation	p.Asn1241Lys(p.N1241K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100672:197100672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8579A>C
AA Mutation	p.Lys2860Thr(p.K2860T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197143157:197143157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375572921
CDS Mutation	c.1095T>G
AA Mutation	p.Ile365Met(p.I365M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197104638:197104638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4613G>A
AA Mutation	p.Arg1538Gln(p.R1538Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197143447:197143447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805G>A
AA Mutation	p.Val269Ile(p.V269I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197102763:197102763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6488A>G
AA Mutation	p.Tyr2163Cys(p.Y2163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197124925:197124925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3113A>G
AA Mutation	p.Asp1038Gly(p.D1038G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197128497:197128497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750015604
CDS Mutation	c.2929C>T
AA Mutation	p.Arg977Cys(p.R977C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197129961:197129961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2583A>G
AA Mutation	p.Ile861Met(p.I861M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197142739:197142739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513A>G
AA Mutation	p.Thr505Ala(p.T505A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197090909:197090909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140679756
CDS Mutation	c.9577C>T
AA Mutation	p.Arg3193Cys(p.R3193C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197090054:197090054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9860G>A
AA Mutation	p.Cys3287Tyr(p.C3287Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197102113:197102113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7138C>T
AA Mutation	p.His2380Tyr(p.H2380Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197102359:197102359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6892G>A
AA Mutation	p.Ala2298Thr(p.A2298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197094139:197094139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9029A>T
AA Mutation	p.Lys3010Ile(p.K3010I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100636:197100636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142176273
CDS Mutation	c.8615C>T
AA Mutation	p.Thr2872Met(p.T2872M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197100546:197100546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8705A>G
AA Mutation	p.Gln2902Arg(p.Q2902R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197104966:197104966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4285T>C
AA Mutation	p.Ser1429Pro(p.S1429P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197090030:197090030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9884C>G
AA Mutation	p.Ala3295Gly(p.A3295G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197103990:197103990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759380732
CDS Mutation	c.5261C>T
AA Mutation	p.Ala1754Val(p.A1754V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197103061:197103061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6190G>A
AA Mutation	p.Ala2064Thr(p.A2064T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197146304:197146304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Cys45Tyr(p.C45Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197142583:197142583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669A>T
AA Mutation	p.Ser557Cys(p.S557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197125072:197125072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780791970
CDS Mutation	c.3056G>A
AA Mutation	p.Arg1019Gln(p.R1019Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197104052:197104052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5199C>G
AA Mutation	p.Ile1733Met(p.I1733M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197101653:197101653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7598C>G
AA Mutation	p.Ser2533Cys(p.S2533C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197128601:197128601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760611432
CDS Mutation	c.2825G>A
AA Mutation	p.Arg942His(p.R942H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197101097:197101097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150872657
CDS Mutation	c.8154A>G
AA Mutation	p.Ile2718Met(p.I2718M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000367409
Start	197101187:197101187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8064G>A
AA Mutation	p.Met2688Ile(p.M2688I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197128591:197128591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2835C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197139813:197139813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151087446
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197142428:197142428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197090208:197090208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9817T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197130000:197130000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2544T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197088406:197088406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10011T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197124227:197124227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3273T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197103401:197103401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537962201
CDS Mutation	c.5850G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197132309:197132309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2463T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197103896:197103896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5355T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367409
Start	197101631:197101631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147160053
CDS Mutation	c.7620A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197104102:197104102(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs199422167
CDS Mutation	c.5149delA
AA Mutation	p.Ile1717Ter(p.I1717*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197124908:197124908(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3130delA
AA Mutation	p.Thr1044LeufsTer8(p.T1044Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197104212:197104212(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5039delA
AA Mutation	p.Asn1680MetfsTer4(p.N1680Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197143515:197143527(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.725_737delGTCGATCTACTAC
AA Mutation	p.Arg242ProfsTer14(p.R242Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197103266:197103266(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5985delA
AA Mutation	p.Ala1996LeufsTer4(p.A1996Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197100980:197100980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.8271delA
AA Mutation	p.Lys2757AsnfsTer2(p.K2757Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197122581:197122582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3404_3405delCA
AA Mutation	p.Thr1135SerfsTer24(p.T1135Sfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	57
Mutation Consequence	stop_gained
Transcription ID	ENST00000367409
Start	197101024:197101024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774702591
CDS Mutation	c.8227C>T
AA Mutation	p.Arg2743Ter(p.R2743*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	58
Mutation Consequence	stop_gained
Transcription ID	ENST00000367409
Start	197124307:197124307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3193C>T
AA Mutation	p.Gln1065Ter(p.Q1065*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197103642:197103643(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5608_5609insCATGCTCTGAA
AA Mutation	p.His1870ProfsTer7(p.H1870Pfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197102395:197102396(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6854_6855dupTC
AA Mutation	p.Lys2286SerfsTer7(p.K2286Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	61
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197105100:197105101(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4150dupA
AA Mutation	p.Ile1384AsnfsTer8(p.I1384Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	62
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367409
Start	197101942:197101943(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.7308dupT
AA Mutation	p.Val2437CysfsTer14(p.V2437Cfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	63
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367409
Start	197129185:197129185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2760+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	64
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000367409
Start	197128667:197128667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2761-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript