Mutation

Primary Site >> Stomach Cancer

Gene >> STC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173317891:173317891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>A
AA Mutation	p.Glu289Lys(p.E289K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173323369:173323369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Gly119Asp(p.G119D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173317924:173317924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Gly278Ser(p.G278S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173325890:173325890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272A>G
AA Mutation	p.Asn91Ser(p.N91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173323370:173323370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Gly119Ser(p.G119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173323409:173323409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769283117
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265087
Start	173328142:173328142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52A>G
AA Mutation	p.Thr18Ala(p.T18A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173325979:173325979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114346665
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173317946:173317946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265087
Start	173328131:173328131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265087
Start	173318087:173318087(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.669delC
AA Mutation	p.Glu224SerfsTer133(p.E224Sfs*133)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript