Mutation

Primary Site >> Stomach Cancer

Gene >> REL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295025
Start	60921834:60921834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159T>C
AA Mutation	p.Tyr387His(p.Y387H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295025
Start	60918224:60918224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141106831
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295025
Start	60918210:60918210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555A>C
AA Mutation	p.Glu185Asp(p.E185D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295025
Start	60891806:60891806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>A
AA Mutation	p.Arg45Gln(p.R45Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295025
Start	60891729:60891729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200474960
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295025
Start	60918204:60918204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574580916
CDS Mutation	c.549T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295025
Start	60920636:60920636(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1086delA
AA Mutation	p.Glu363AsnfsTer11(p.E363Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295025
Start	60917018:60917018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript