Colon Cancer: Gene >> KLRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381902
Start	10435345:10435345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752097000
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381902
Start	10431208:10431208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>T
AA Mutation	p.Ala202Val(p.A202V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381902
Start	10435933:10435933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000381902
Start	10431117:10431117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000381902
Start	10435929:10435929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>T
AA Mutation	p.Gln20Ter(p.Q20*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLRC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381902
Start	10432124:10432124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566G>C
AA Mutation	p.Gly189Ala(p.G189A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript