Colon Cancer: Gene >> EIF3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2377002:2377002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081A>G
AA Mutation	p.Asn694Ser(p.N694S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2369664:2369664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1596G>C
AA Mutation	p.Arg532Ser(p.R532S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2360837:2360837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627G>T
AA Mutation	p.Lys209Asn(p.K209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2375396:2375396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766601514
CDS Mutation	c.1897G>A
AA Mutation	p.Gly633Ser(p.G633S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2363704:2363704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772725989
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2377024:2377024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2103G>C
AA Mutation	p.Gln701His(p.Q701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2379474:2379474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2422A>G
AA Mutation	p.Ile808Val(p.I808V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2377055:2377055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134C>A
AA Mutation	p.Leu712Met(p.L712M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2366430:2366430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2379153:2379153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375864470
CDS Mutation	c.2252G>A
AA Mutation	p.Arg751His(p.R751H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2378740:2378740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206C>T
AA Mutation	p.Arg736Cys(p.R736C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360876
Start	2379458:2379458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2406C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000360876
Start	2371850:2371850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1687+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360876
Start	2371797:2371797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635A>C
AA Mutation	p.Glu545Asp(p.E545D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript