Colon Cancer: Gene >> LOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122077910:122077910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76G>A
AA Mutation	p.Ala26Thr(p.A26T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122075521:122075521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761T>C
AA Mutation	p.Val254Ala(p.V254A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122077937:122077937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122077967:122077967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19G>A
AA Mutation	p.Val7Met(p.V7M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122075440:122075440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>A
AA Mutation	p.Arg281Gln(p.R281Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122077622:122077622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566461481
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Cys(p.R122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231004
Start	122077410:122077410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000231004
Start	122070052:122070052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LOX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231004
Start	122075440:122075440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>A
AA Mutation	p.Arg281Gln(p.R281Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231004
Start	122075427:122075427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.855C>A
Mutation Classification	Silent
Feature Type	Transcript