Mutation

Primary Site >> Stomach Cancer

Gene >> EEF1D

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143586256:143586256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751616584
CDS Mutation	c.152C>T
AA Mutation	p.Ala51Val(p.A51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143581262:143581262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256A>G
AA Mutation	p.Ser86Gly(p.S86G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143579812:143579812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199856046
CDS Mutation	c.826G>A
AA Mutation	p.Ala276Thr(p.A276T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143580055:143580055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764G>A
AA Mutation	p.Gly255Glu(p.G255E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143581235:143581235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Cys(p.R95C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143580526:143580526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592A>G
AA Mutation	p.Ile198Val(p.I198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317198
Start	143581069:143581069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138645618
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317198
Start	143580105:143580105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	splice_donor_variant;splice_acceptor_variant;intron_variant
Transcription ID	ENST00000317198
Start	143581155:143581228(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.290-1_289+1delGTGAGGCCCCGGGCCAGTGGGTTGGGGCTGTCCCTGGCCCCTGCCATCTAACCGTGCTCCCCTTGCCCCCCCAG
Mutation Classification	Splice_Site
Feature Type	Transcript