Mutation

Primary Site >> Stomach Cancer

Gene >> THBS4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80070715:80070715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371339729
CDS Mutation	c.1525G>A
AA Mutation	p.Glu509Lys(p.E509K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350881
Start	80079905:80079905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2512G>A
AA Mutation	p.Ala838Thr(p.A838T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80055836:80055836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760093592
CDS Mutation	c.344A>G
AA Mutation	p.Asn115Ser(p.N115S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80035553:80035553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Gly6Arg(p.G6R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80080050:80080050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2657A>G
AA Mutation	p.Gln886Arg(p.Q886R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80071138:80071138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678G>A
AA Mutation	p.Asp560Asn(p.D560N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80059850:80059850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>T
AA Mutation	p.Gly311Val(p.G311V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80083122:80083122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2867T>G
AA Mutation	p.Phe956Cys(p.F956C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80082416:80082416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2695T>C
AA Mutation	p.Tyr899His(p.Y899H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80072359:80072359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802C>T
AA Mutation	p.Ala601Val(p.A601V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80072346:80072346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789G>T
AA Mutation	p.Gly597Cys(p.G597C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80082471:80082471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760330965
CDS Mutation	c.2750G>A
AA Mutation	p.Arg917His(p.R917H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80059825:80059825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34249634
CDS Mutation	c.907G>A
AA Mutation	p.Asp303Asn(p.D303N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80072328:80072328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148589675
CDS Mutation	c.1771C>T
AA Mutation	p.Arg591Trp(p.R591W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80071136:80071136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1676G>A
AA Mutation	p.Gly559Glu(p.G559E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000350881
Start	80059781:80059781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779865957
CDS Mutation	c.863G>A
AA Mutation	p.Arg288His(p.R288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80070651:80070651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80059749:80059749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567115646
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80077002:80077002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779486193
CDS Mutation	c.2040A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350881
Start	80061724:80061724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350881
Start	80056017:80056017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.526delC
AA Mutation	p.Gln176ArgfsTer11(p.Q176Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350881
Start	80076991:80076991(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2033delC
AA Mutation	p.Pro678LeufsTer50(p.P678Lfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript