Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DDX20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111766051:111766051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753843841
CDS Mutation	c.1627G>A
AA Mutation	p.Glu543Lys(p.E543K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111766245:111766245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1821G>T
AA Mutation	p.Glu607Asp(p.E607D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111760767:111760767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773108633
CDS Mutation	c.742G>A
AA Mutation	p.Glu248Lys(p.E248K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111765844:111765844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420A>C
AA Mutation	p.Lys474Gln(p.K474Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111756708:111756708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364G>A
AA Mutation	p.Asp122Asn(p.D122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369702
Start	111762700:111762700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369702
Start	111766674:111766674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2250C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369702
Start	111762706:111762706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DDX20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111760767:111760767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773108633
CDS Mutation	c.742G>A
AA Mutation	p.Glu248Lys(p.E248K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111766712:111766712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2288G>A
AA Mutation	p.Arg763His(p.R763H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369702
Start	111766525:111766525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101A>C
AA Mutation	p.Asn701His(p.N701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript