Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KLRB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229402
Start	9598068:9598068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747037091
CDS Mutation	c.508G>A
AA Mutation	p.Gly170Ser(p.G170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229402
Start	9598580:9598580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769790958
CDS Mutation	c.333T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229402
Start	9598502:9598502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000229402
Start	9598537:9598537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>T
AA Mutation	p.Glu126Ter(p.E126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLRB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229402
Start	9607782:9607782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.58A>T
AA Mutation	p.Ser20Cys(p.S20C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229402
Start	9607758:9607758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750757177
CDS Mutation	c.82C>T
AA Mutation	p.Arg28Trp(p.R28W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000229402
Start	9598076:9598076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Trp167Ter(p.W167*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000229402
Start	9595315:9595315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>T
AA Mutation	p.Glu213Ter(p.E213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript