Colon Cancer: Gene >> CSNK2A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	487567:487567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833G>A
AA Mutation	p.Arg278Gln(p.R278Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	486447:486447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989A>T
AA Mutation	p.Asp330Val(p.D330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	497727:497727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420T>G
AA Mutation	p.Ile140Met(p.I140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	499910:499910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777370152
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Cys(p.R80C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	488691:488691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811G>T
AA Mutation	p.Asp271Tyr(p.D271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	483983:483983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154C>A
AA Mutation	p.Ala385Asp(p.A385D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217244
Start	487552:487552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848G>A
AA Mutation	p.Arg283His(p.R283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217244
Start	487464:487464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CSNK2A1

No Mutation Annotation!