Mutation

Primary Site >> Stomach Cancer

Gene >> ELN

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358929
Start	74043918:74043918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467C>A
AA Mutation	p.Pro156Gln(p.P156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358929
Start	74063168:74063168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988G>A
AA Mutation	p.Gly663Glu(p.G663E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74043904:74043904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74045262:74045262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74042618:74042618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74048519:74048519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74063658:74063658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2142C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74042988:74042988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74057446:74057446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74047691:74047691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358929
Start	74059941:74059941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576324025
CDS Mutation	c.1557T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358929
Start	74065970:74065970(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2249delG
AA Mutation	p.Gly750ValfsTer63(p.G750Vfs*63)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358929
Start	74046710:74046710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.590delG
AA Mutation	p.Gly197AspfsTer126(p.G197Dfs*126)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript