Mutation

Primary Site >> Stomach Cancer

Gene >> CXXC5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302517
Start	139681421:139681421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898A>G
AA Mutation	p.Lys300Glu(p.K300E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302517
Start	139681109:139681109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>A
AA Mutation	p.Val196Met(p.V196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302517
Start	139681332:139681332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302517
Start	139681133:139681133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610G>T
AA Mutation	p.Gly204Cys(p.G204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302517
Start	139681237:139681237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371318261
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302517
Start	139681033:139681033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302517
Start	139680757:139680757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745505391
CDS Mutation	c.234G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302517
Start	139681138:139681138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302517
Start	139680686:139680686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.168delC
AA Mutation	p.Glu57SerfsTer40(p.E57Sfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript