Colon Cancer: Gene >> CHKA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265689
Start	68070273:68070273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785G>T
AA Mutation	p.Arg262Ile(p.R262I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265689
Start	68070256:68070256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265689
Start	68070804:68070804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHKA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265689
Start	68064555:68064555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202T>G
AA Mutation	p.Ile401Arg(p.I401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265689
Start	68081433:68081433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527271212
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265689
Start	68074822:68074822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525G>T
AA Mutation	p.Glu175Asp(p.E175D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265689
Start	68074738:68074738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript