Mutation

Primary Site >> Stomach Cancer

Gene >> USP9X

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41210534:41210534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5041C>T
AA Mutation	p.Arg1681Cys(p.R1681C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41167551:41167551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398C>T
AA Mutation	p.Leu800Phe(p.L800F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41216542:41216542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5975G>A
AA Mutation	p.Arg1992Gln(p.R1992Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41186614:41186614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3656T>C
AA Mutation	p.Val1219Ala(p.V1219A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324545
Start	41223219:41223219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6568G>A
AA Mutation	p.Val2190Met(p.V2190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41165880:41165880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1994T>C
AA Mutation	p.Leu665Ser(p.L665S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41201108:41201108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4652G>A
AA Mutation	p.Arg1551His(p.R1551H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41167523:41167523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2370A>G
AA Mutation	p.Ile790Met(p.I790M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41166118:41166118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2232C>G
AA Mutation	p.Phe744Leu(p.F744L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41162862:41162862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1970G>A
AA Mutation	p.Arg657Gln(p.R657Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41210573:41210573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5080G>A
AA Mutation	p.Val1694Met(p.V1694M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41141364:41141364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094T>C
AA Mutation	p.Val365Ala(p.V365A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41143381:41143381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252C>T
AA Mutation	p.Arg418Cys(p.R418C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41168091:41168091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2509A>G
AA Mutation	p.Lys837Glu(p.K837E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41216389:41216389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374231846
CDS Mutation	c.5822G>A
AA Mutation	p.Arg1941His(p.R1941H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41170006:41170006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2648G>C
AA Mutation	p.Gly883Ala(p.G883A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000324545
Start	41134778:41134778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376A>C
AA Mutation	p.Ile126Leu(p.I126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324545
Start	41229788:41229788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7440A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324545
Start	41136962:41136962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324545
Start	41168189:41168189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2607T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324545
Start	41140751:41140751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771426271
CDS Mutation	c.750A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324545
Start	41123704:41123704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.82delC
AA Mutation	p.Leu28SerfsTer51(p.L28Sfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000324545
Start	41166134:41166134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2248C>T
AA Mutation	p.Arg750Ter(p.R750*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000324545
Start	41141171:41141171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976G>T
AA Mutation	p.Glu326Ter(p.E326*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000324545
Start	41166110:41166110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2224C>T
AA Mutation	p.Arg742Ter(p.R742*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324545
Start	41153083:41153083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1897+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324545
Start	41184130:41184130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3279+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript