Mutation

Primary Site >> Stomach Cancer

Gene >> EZR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337147
Start	158785484:158785484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292A>G
AA Mutation	p.Thr98Ala(p.T98A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337147
Start	158784720:158784720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>A
AA Mutation	p.Asp159Asn(p.D159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337147
Start	158784707:158784707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>G
AA Mutation	p.Leu163Arg(p.L163R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337147
Start	158783563:158783563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>C
AA Mutation	p.Gly219Arg(p.G219R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337147
Start	158770858:158770858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183636404
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000337147
Start	158785420:158785420(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.356delC
AA Mutation	p.Pro119LeufsTer34(p.P119Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	7
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000337147
Start	158785283:158785319(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.457_467+26delATCCCTCAAAGGTGAGCACAGGATGACCCGGCCTGGG
Mutation Classification	Splice_Site
Feature Type	Transcript