Mutation

Primary Site >> Stomach Cancer

Gene >> SPARCL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87482546:87482546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767426721
CDS Mutation	c.1546A>G
AA Mutation	p.Thr516Ala(p.T516A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87490783:87490783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387C>A
AA Mutation	p.Pro463Thr(p.P463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87473798:87473798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972A>G
AA Mutation	p.Ile658Val(p.I658V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87495066:87495066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116A>G
AA Mutation	p.Asn39Ser(p.N39S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493740:87493740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060A>G
AA Mutation	p.Arg354Gly(p.R354G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282470
Start	87493760:87493760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.Asp347Gly(p.D347G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282470
Start	87493765:87493765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373342606
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282470
Start	87494378:87494378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.422delT
AA Mutation	p.Leu141TrpfsTer35(p.L141Wfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282470
Start	87499555:87499555(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.20delT
AA Mutation	p.Phe7SerfsTer29(p.F7Sfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript