Colon Cancer: Gene >> EBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000495186
Start	48527208:48527208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.392C>T
AA Mutation	p.Pro131Leu(p.P131L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000495186
Start	48528275:48528275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141925556
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Cys(p.R171C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000495186
Start	48528377:48528377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>T
AA Mutation	p.Leu205Phe(p.L205F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000495186
Start	48527256:48527256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28935174
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000495186
Start	48524032:48524032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145509273
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000495186
Start	48528263:48528263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000495186
Start	48528386:48528386(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.622delG
AA Mutation	p.Val208Ter(p.V208*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000495186
Start	48527210:48527210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394C>T
AA Mutation	p.Leu132Phe(p.L132F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript