Mutation

Primary Site >> Stomach Cancer

Gene >> NUP98

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3760616:3760616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097G>A
AA Mutation	p.Gly366Asp(p.G366D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676346:3676346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763063541
CDS Mutation	c.5267G>A
AA Mutation	p.Arg1756His(p.R1756H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3695477:3695477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201757730
CDS Mutation	c.4190G>A
AA Mutation	p.Arg1397His(p.R1397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676344:3676344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761211053
CDS Mutation	c.5269G>A
AA Mutation	p.Val1757Met(p.V1757M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676239:3676239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5374A>G
AA Mutation	p.Met1792Val(p.M1792V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3679693:3679693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4985A>G
AA Mutation	p.Glu1662Gly(p.E1662G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676289:3676289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5324C>A
AA Mutation	p.Pro1775His(p.P1775H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3700676:3700676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3727G>A
AA Mutation	p.Val1243Ile(p.V1243I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3773685:3773685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550A>G
AA Mutation	p.Thr184Ala(p.T184A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3691452:3691452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4400T>G
AA Mutation	p.Leu1467Arg(p.L1467R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676209:3676209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765252401
CDS Mutation	c.5404C>T
AA Mutation	p.Arg1802Cys(p.R1802C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3779223:3779223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111T>G
AA Mutation	p.Phe37Leu(p.F37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3691410:3691410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4442A>C
AA Mutation	p.Glu1481Ala(p.E1481A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3712578:3712578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2779G>A
AA Mutation	p.Ala927Thr(p.A927T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3693335:3693335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4259C>T
AA Mutation	p.Ser1420Phe(p.S1420F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3723445:3723445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1909C>A
AA Mutation	p.Leu637Ile(p.L637I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3723355:3723355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999A>T
AA Mutation	p.Ile667Phe(p.I667F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3702724:3702724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3302C>T
AA Mutation	p.Ala1101Val(p.A1101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3683235:3683235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4934G>A
AA Mutation	p.Arg1645His(p.R1645H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3775892:3775892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485T>A
AA Mutation	p.Ile162Asn(p.I162N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3723315:3723315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2039A>G
AA Mutation	p.Asn680Ser(p.N680S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3782104:3782104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Ser5Leu(p.S5L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3676272:3676272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766745271
CDS Mutation	c.5341C>T
AA Mutation	p.Arg1781Cys(p.R1781C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000359171
Start	3705299:3705299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144100440
CDS Mutation	c.3034C>T
AA Mutation	p.Arg1012Cys(p.R1012C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359171
Start	3691466:3691466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141039100
CDS Mutation	c.4386T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359171
Start	3686086:3686086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4614C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359171
Start	3768677:3768677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359171
Start	3695545:3695545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4122G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359171
Start	3771857:3771857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000359171
Start	3699238:3699238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3904C>T
AA Mutation	p.Arg1302Ter(p.R1302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359171
Start	3775956:3775957(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.420dupT
AA Mutation	p.Gly141TrpfsTer12(p.G141Wfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript