Colon Cancer: Gene >> LILRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54274768:54274768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571Lys(p.R571K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54279546:54279546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457T>A
AA Mutation	p.Phe153Ile(p.F153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54280291:54280291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>A
AA Mutation	p.Leu15Met(p.L15M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54274775:54274775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1705A>G
AA Mutation	p.Thr569Ala(p.T569A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54279970:54279970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141797988
CDS Mutation	c.176G>A
AA Mutation	p.Arg59His(p.R59H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54278917:54278917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Gly284Cys(p.G284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54278946:54278946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54279438:54279438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565A>G
AA Mutation	p.Asn189Asp(p.N189D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54276839:54276839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1451G>A
AA Mutation	p.Arg484Gln(p.R484Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54279435:54279435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54280013:54280013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775537731
CDS Mutation	c.133G>A
AA Mutation	p.Val45Ile(p.V45I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391749
Start	54278348:54278348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373595683
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391749
Start	54278549:54278549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391749
Start	54277915:54277915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1283delC
AA Mutation	p.Pro428HisfsTer35(p.P428Hfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LILRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391749
Start	54274819:54274819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1661C>A
AA Mutation	p.Ser554Tyr(p.S554Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript