Colon Cancer: Gene >> HMBS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119090045:119090045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>A
AA Mutation	p.Leu134Ile(p.L134I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119092767:119092767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781T>G
AA Mutation	p.Cys261Gly(p.C261G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119092785:119092785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>A
AA Mutation	p.Val267Met(p.V267M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119093013:119093013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904C>A
AA Mutation	p.Pro302Thr(p.P302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119088642:119088642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746673847
CDS Mutation	c.95G>A
AA Mutation	p.Arg32His(p.R32H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278715
Start	119092967:119092967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778353358
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HMBS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278715
Start	119092149:119092149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637T>C
AA Mutation	p.Tyr213His(p.Y213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript