Mutation

Primary Site >> Stomach Cancer

Gene >> SNX1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64127233:64127233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Trp(p.R238W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64129923:64129923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779132736
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64130255:64130255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>C
AA Mutation	p.Glu317Gln(p.E317Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000559844
Start	64131891:64131891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370174132
CDS Mutation	c.1220G>A
AA Mutation	p.Arg407His(p.R407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64126130:64126130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562A>G
AA Mutation	p.Ser188Gly(p.S188G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64118807:64118807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770784911
CDS Mutation	c.419A>G
AA Mutation	p.Glu140Gly(p.E140G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000559844
Start	64131872:64131872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768722767
CDS Mutation	c.1201C>T
AA Mutation	p.Arg401Cys(p.R401C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000559844
Start	64131758:64131758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000559844
Start	64127254:64127254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript