Colon Cancer: Gene >> CKAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378026
Start	106239739:106239739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141394460
CDS Mutation	c.1094G>A
AA Mutation	p.Arg365His(p.R365H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378026
Start	106240229:106240229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376479872
CDS Mutation	c.604G>A
AA Mutation	p.Glu202Lys(p.E202K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378026
Start	106239645:106239645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758624024
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CKAP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378026
Start	106239781:106239781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052C>G
AA Mutation	p.Ala351Gly(p.A351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378026
Start	106239352:106239352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481G>T
AA Mutation	p.Gly494Val(p.G494V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378026
Start	106239854:106239854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769777070
CDS Mutation	c.979G>A
AA Mutation	p.Glu327Lys(p.E327K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript