Colon Cancer: Gene >> LILRB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391736
Start	54663058:54663058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25C>T
AA Mutation	p.Leu9Phe(p.L9F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391736
Start	54666246:54666246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777315383
CDS Mutation	c.881G>A
AA Mutation	p.Arg294Lys(p.R294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391736
Start	54665844:54665844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371595706
CDS Mutation	c.787G>A
AA Mutation	p.Gly263Arg(p.G263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391736
Start	54663993:54663993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370306475
CDS Mutation	c.310G>A
AA Mutation	p.Val104Ile(p.V104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391736
Start	54664397:54664397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369944780
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391736
Start	54664397:54664398(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.573dupG
AA Mutation	p.Thr192AspfsTer20(p.T192Dfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LILRB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391736
Start	54663967:54663967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284G>T
AA Mutation	p.Arg95Ile(p.R95I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript