Mutation

Primary Site >> Stomach Cancer

Gene >> CYBB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37792026:37792026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304A>G
AA Mutation	p.Lys102Glu(p.K102E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37795999:37795999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532A>G
AA Mutation	p.Thr178Ala(p.T178A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37799035:37799035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Gly252Glu(p.G252E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37805103:37805103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782094658
CDS Mutation	c.1249G>A
AA Mutation	p.Ala417Thr(p.A417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37804115:37804115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136C>T
AA Mutation	p.Ala379Val(p.A379V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37801283:37801283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832T>G
AA Mutation	p.Phe278Val(p.F278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37782109:37782109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781986436
CDS Mutation	c.67G>A
AA Mutation	p.Val23Ile(p.V23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37804051:37804051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781992322
CDS Mutation	c.1072G>A
AA Mutation	p.Val358Ile(p.V358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37804012:37804012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>A
AA Mutation	p.Ala345Thr(p.A345T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378588
Start	37806446:37806446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000378588
Start	37791993:37791993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript