Colon Cancer: Gene >> BGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153508396:153508396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368783683
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353His(p.R353H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153506071:153506071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560G>A
AA Mutation	p.Cys187Tyr(p.C187Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331595
Start	153506923:153506923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770G>T
AA Mutation	p.Arg257Met(p.R257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153504678:153504678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47C>A
AA Mutation	p.Ala16Asp(p.A16D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153506537:153506537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782602954
CDS Mutation	c.574G>A
AA Mutation	p.Gly192Arg(p.G192R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153505909:153505909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.398C>T
AA Mutation	p.Ala133Val(p.A133V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153506005:153506005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494G>A
AA Mutation	p.Arg165His(p.R165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153506904:153506904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>T
AA Mutation	p.Arg251Cys(p.R251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153505304:153505304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305T>C
AA Mutation	p.Ile102Thr(p.I102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331595
Start	153506006:153506006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153505888:153505888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377T>A
AA Mutation	p.Ile126Asn(p.I126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331595
Start	153505923:153505923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript