Colon Cancer: Gene >> HBD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380299
Start	5234118:5234118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>T
AA Mutation	p.Ala63Val(p.A63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380299
Start	5233068:5233068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340G>A
AA Mutation	p.Val114Met(p.V114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380299
Start	5234164:5234164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>A
AA Mutation	p.Asp48Asn(p.D48N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380299
Start	5232994:5232994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380299
Start	5234051:5234051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255T>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HBD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380299
Start	5234180:5234180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>A
AA Mutation	p.Phe42Leu(p.F42L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380299
Start	5232985:5232985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript