Colon Cancer: Gene >> CAMK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9761493:9761493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600T>G
AA Mutation	p.Asp200Glu(p.D200E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9763002:9763002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341C>T
AA Mutation	p.Thr114Met(p.T114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9761510:9761510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583T>C
AA Mutation	p.Tyr195His(p.Y195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9763026:9763026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746723292
CDS Mutation	c.317G>A
AA Mutation	p.Arg106His(p.R106H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9761701:9761701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>A
AA Mutation	p.Asp162Glu(p.D162E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256460
Start	9761635:9761635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145978414
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256460
Start	9761674:9761674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746152391
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256460
Start	9760696:9760696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143557505
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CAMK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9761752:9761752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435G>T
AA Mutation	p.Glu145Asp(p.E145D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256460
Start	9759745:9759745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751G>T
AA Mutation	p.Asp251Tyr(p.D251Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript