Colon Cancer: Gene >> CSK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74801049:74801049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749945630
CDS Mutation	c.760G>A
AA Mutation	p.Val254Met(p.V254M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74801753:74801753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946G>A
AA Mutation	p.Ala316Thr(p.A316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74801763:74801763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956A>G
AA Mutation	p.Asn319Ser(p.N319S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74800882:74800882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754136671
CDS Mutation	c.682G>A
AA Mutation	p.Ala228Thr(p.A228T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74798863:74798863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200009296
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220003
Start	74798861:74798861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000220003
Start	74802469:74802469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309C>T
AA Mutation	p.Arg437Ter(p.R437*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CSK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220003
Start	74801759:74801759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952C>T
AA Mutation	p.Arg318Cys(p.R318C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000220003
Start	74800923:74800923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript