Mutation

Primary Site >> Stomach Cancer

Gene >> NCKIPSD

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48674647:48674647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066G>A
AA Mutation	p.Arg689His(p.R689H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48679385:48679385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562C>T
AA Mutation	p.Ala521Val(p.A521V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48680122:48680122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200T>G
AA Mutation	p.Ser400Arg(p.S400R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48679670:48679670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394G>A
AA Mutation	p.Gly465Asp(p.G465D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48680091:48680091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760490512
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Cys(p.R411C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294129
Start	48674708:48674708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750894262
CDS Mutation	c.2005C>T
AA Mutation	p.Arg669Cys(p.R669C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294129
Start	48681422:48681422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000294129
Start	48679800:48679800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript