Mutation

Primary Site >> Stomach Cancer

Gene >> POSTN

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37587829:37587829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599C>A
AA Mutation	p.Pro200His(p.P200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37579974:37579974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547T>G
AA Mutation	p.Leu516Arg(p.L516R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37586156:37586156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878A>G
AA Mutation	p.Asp293Gly(p.D293G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37587887:37587887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541A>C
AA Mutation	p.Asn181His(p.N181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37563343:37563343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200287900
CDS Mutation	c.2501G>A
AA Mutation	p.Arg834His(p.R834H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37582370:37582370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373753100
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463His(p.R463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37579329:37579329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691T>G
AA Mutation	p.Leu564Arg(p.L564R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37586195:37586195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839A>T
AA Mutation	p.Glu280Val(p.E280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37579872:37579872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649A>T
AA Mutation	p.Glu550Val(p.E550V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37598630:37598630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Cys(p.R33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37584737:37584737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777895150
CDS Mutation	c.1087C>A
AA Mutation	p.Gln363Lys(p.Q363K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37584860:37584860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>A
AA Mutation	p.Glu322Lys(p.E322K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37579353:37579353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1667A>T
AA Mutation	p.Lys556Ile(p.K556I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37580612:37580612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1478A>G
AA Mutation	p.Lys493Arg(p.K493R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000379747
Start	37584874:37584874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950G>C
AA Mutation	p.Gly317Ala(p.G317A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37582423:37582423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37574609:37574609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37597249:37597249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37586263:37586263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750527557
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37579113:37579113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766902123
CDS Mutation	c.1800T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37592140:37592140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37584057:37584057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368157999
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37579958:37579958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379747
Start	37590474:37590474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379747
Start	37570653:37570653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2196delA
AA Mutation	p.Lys732AsnfsTer13(p.K732Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379747
Start	37587886:37587886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.542delA
AA Mutation	p.Asn181MetfsTer3(p.N181Mfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379747
Start	37597205:37597205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.197delA
AA Mutation	p.Lys66SerfsTer19(p.K66Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379747
Start	37598713:37598713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.14delT
AA Mutation	p.Leu5TyrfsTer15(p.L5Yfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript