Colon Cancer: Gene >> KIR3DL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391728
Start	54818419:54818419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175A>G
AA Mutation	p.Met59Val(p.M59V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391728
Start	54819856:54819856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779085160
CDS Mutation	c.499C>T
AA Mutation	p.Leu167Phe(p.L167F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391728
Start	54816526:54816526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26C>T
AA Mutation	p.Ala9Val(p.A9V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391728
Start	54818352:54818352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391728
Start	54817562:54817562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391728
Start	54819942:54819942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KIR3DL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391728
Start	54830178:54830178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413His(p.R413H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391728
Start	54830266:54830266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326C>A
Mutation Classification	Silent
Feature Type	Transcript