Colon Cancer: Gene >> EIF4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53039264:53039264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603G>T
AA Mutation	p.Ala535Ser(p.A535S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53037603:53037603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1501G>C
AA Mutation	p.Glu501Gln(p.E501Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53028132:53028132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758683560
CDS Mutation	c.923G>A
AA Mutation	p.Arg308Gln(p.R308Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53033991:53033991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747657993
CDS Mutation	c.1165C>T
AA Mutation	p.Arg389Cys(p.R389C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53027793:53027793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53018911:53018911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Arg89Ser(p.R89S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262056
Start	53034626:53034626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753615463
CDS Mutation	c.1223G>A
AA Mutation	p.Arg408Gln(p.R408Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000262056
Start	53033808:53033808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.988delC
AA Mutation	p.Gln330LysfsTer5(p.Q330Kfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000262056
Start	53039240:53039240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579G>T
AA Mutation	p.Glu527Ter(p.E527*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000262056
Start	53027895:53027895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Ter(p.R261*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF4B

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000262056
Start	53018995:53018995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Ter(p.R117*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000262056
Start	53033949:53033949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123G>T
AA Mutation	p.Glu375Ter(p.E375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript