Colon Cancer: Gene >> EIF4A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269349
Start	80136300:80136300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019G>A
AA Mutation	p.Gly340Glu(p.G340E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269349
Start	80139110:80139110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639G>T
AA Mutation	p.Gln213His(p.Q213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269349
Start	80140016:80140016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497G>A
AA Mutation	p.Arg166His(p.R166H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269349
Start	80138254:80138254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755A>T
AA Mutation	p.Lys252Met(p.K252M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269349
Start	80139027:80139027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>G
AA Mutation	p.Val241Gly(p.V241G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269349
Start	80139080:80139080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535401553
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269349
Start	80144177:80144177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747892909
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EIF4A3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269349
Start	80138244:80138244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61756263
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269349
Start	80139029:80139029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720G>A
Mutation Classification	Silent
Feature Type	Transcript