Colon Cancer: Gene >> DDX28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68022184:68022184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019T>C
AA Mutation	p.Leu340Ser(p.L340S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68021802:68021802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1401G>T
AA Mutation	p.Glu467Asp(p.E467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68022847:68022847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356T>C
AA Mutation	p.Val119Ala(p.V119A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	start_lost
Transcription ID	ENST00000332395
Start	68023200:68023200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DDX28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68021650:68021650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553C>T
AA Mutation	p.Ala518Val(p.A518V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68022010:68022010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1193G>T
AA Mutation	p.Gly398Val(p.G398V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332395
Start	68022670:68022670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533A>G
AA Mutation	p.Lys178Arg(p.K178R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript