Colon Cancer: Gene >> LTB4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345363
Start	24315748:24315748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97C>G
AA Mutation	p.Leu33Val(p.L33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345363
Start	24315914:24315914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263C>T
AA Mutation	p.Ala88Val(p.A88V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345363
Start	24316677:24316677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345363
Start	24315676:24315676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.30delC
AA Mutation	p.Ser11HisfsTer2(p.S11Hfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LTB4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345363
Start	24316219:24316219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568T>G
AA Mutation	p.Phe190Val(p.F190V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345363
Start	24315872:24315872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221T>C
AA Mutation	p.Phe74Ser(p.F74S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript