Colon Cancer: Gene >> EIF3I

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373586
Start	32228766:32228766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759750490
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Trp(p.R227W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373586
Start	32224467:32224467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.242G>A
AA Mutation	p.Cys81Tyr(p.C81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373586
Start	32224085:32224085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148G>T
AA Mutation	p.Gly50Cys(p.G50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373586
Start	32228587:32228587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762483424
CDS Mutation	c.617C>T
AA Mutation	p.Ala206Val(p.A206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373586
Start	32231122:32231122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904A>G
AA Mutation	p.Ser302Gly(p.S302G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373586
Start	32226178:32226178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373586
Start	32226223:32226223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373586
Start	32222615:32222615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373586
Start	32230967:32230967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.845delA
AA Mutation	p.Lys282ArgfsTer76(p.K282Rfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EIF3I

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373586
Start	32226259:32226259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373586
Start	32226476:32226476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript