Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EIF2S3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253039
Start	24073097:24073097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189A>G
AA Mutation	p.Lys397Glu(p.K397E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253039
Start	24062458:24062458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521T>C
AA Mutation	p.Leu174Pro(p.L174P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253039
Start	24057692:24057692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253039
Start	24068011:24068011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253039
Start	24073223:24073224(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1321dupA
AA Mutation	p.Ile441AsnfsTer4(p.I441Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EIF2S3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253039
Start	24073098:24073098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190A>G
AA Mutation	p.Lys397Arg(p.K397R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253039
Start	24068099:24068099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>A
AA Mutation	p.Gly335Ser(p.G335S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253039
Start	24064291:24064291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728T>C
AA Mutation	p.Ile243Thr(p.I243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253039
Start	24062453:24062453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516A>G
Mutation Classification	Silent
Feature Type	Transcript