Colon Cancer: Gene >> EEF1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309268
Start	73518152:73518152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142G>A
AA Mutation	p.Arg381His(p.R381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309268
Start	73519390:73519390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309268
Start	73518714:73518714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756T>G
AA Mutation	p.Asp252Glu(p.D252E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309268
Start	73519153:73519153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>G
AA Mutation	p.Arg134Gly(p.R134G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309268
Start	73519199:73519199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309268
Start	73518595:73518595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.788delC
AA Mutation	p.Pro263LeufsTer27(p.P263Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EEF1A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309268
Start	73518161:73518161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133A>C
AA Mutation	p.Lys378Thr(p.K378T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_lost
Transcription ID	ENST00000309268
Start	73517812:73517812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387T>C
AA Mutation	p.Ter463ArgextTer66(p.*463Rext*66)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript