Colon Cancer: Gene >> EEF1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143586224:143586224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Ala62Thr(p.A62T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143580579:143580579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200146410
CDS Mutation	c.539G>A
AA Mutation	p.Arg180Gln(p.R180Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317198
Start	143580696:143580696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>A
AA Mutation	p.Pro141Gln(p.P141Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317198
Start	143581087:143581087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317198
Start	143580131:143580131(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.688delG
AA Mutation	p.Ala230LeufsTer55(p.A230Lfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000317198
Start	143580042:143580044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.775_777delCTG
AA Mutation	p.Leu259del(p.L259del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EEF1D

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317198
Start	143581287:143581287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370722668
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript