Colon Cancer: Gene >> EAPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250454
Start	34516368:34516368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800C>T
AA Mutation	p.Ala267Val(p.A267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250454
Start	34533449:34533449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347G>T
AA Mutation	p.Arg116Ile(p.R116I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250454
Start	34516332:34516332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149923274
CDS Mutation	c.836A>G
AA Mutation	p.Asn279Ser(p.N279S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250454
Start	34516335:34516335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.833delT
AA Mutation	p.Phe278SerfsTer4(p.F278Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EAPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250454
Start	34516458:34516458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>A
AA Mutation	p.Ser237Tyr(p.S237Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript