Colon Cancer: Gene >> LRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538460:4538460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138157436
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538262:4538262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722T>C
AA Mutation	p.Leu241Pro(p.L241P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538713:4538713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750105391
CDS Mutation	c.271G>A
AA Mutation	p.Ala91Thr(p.A91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538535:4538535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.449A>G
AA Mutation	p.Asn150Ser(p.N150S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538244:4538244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740A>G
AA Mutation	p.Lys247Arg(p.K247R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306390
Start	4538603:4538603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306390
Start	4538276:4538276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200554386
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306390
Start	4538834:4538834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306390
Start	4538441:4538441(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.543delC
AA Mutation	p.Leu183CysfsTer26(p.L183Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306390
Start	4538942:4538943(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.41dupG
AA Mutation	p.Ile15HisfsTer7(p.I15Hfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306390
Start	4538412:4538412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754452460
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306390
Start	4538657:4538657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567253168
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript