Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CPOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98591111:98591111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>A
AA Mutation	p.Glu201Lys(p.E201K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98585538:98585538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075A>G
AA Mutation	p.Arg359Gly(p.R359G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98580708:98580708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200810233
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98580725:98580725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323A>C
AA Mutation	p.Glu441Asp(p.E441D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98585630:98585630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749579807
CDS Mutation	c.983G>A
AA Mutation	p.Arg328His(p.R328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264193
Start	98580698:98580698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264193
Start	98585519:98585519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094A>G
AA Mutation	p.Tyr365Cys(p.Y365C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264193
Start	98593157:98593157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264193
Start	98585578:98585578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752340562
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript