Colon Cancer: Gene >> LRIG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58874272:58874272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2898G>T
AA Mutation	p.Lys966Asn(p.K966N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58887794:58887794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086G>T
AA Mutation	p.Lys362Asn(p.K362N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58888445:58888445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>T
AA Mutation	p.Glu277Asp(p.E277D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58876484:58876484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2656T>C
AA Mutation	p.Ser886Pro(p.S886P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58886872:58886872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1110A>C
AA Mutation	p.Glu370Asp(p.E370D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58888368:58888368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908G>A
AA Mutation	p.Ser303Asn(p.S303N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58877442:58877442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2494C>A
AA Mutation	p.His832Asn(p.H832N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58880850:58880850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532T>C
AA Mutation	p.Ile511Thr(p.I511T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58880748:58880748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634A>G
AA Mutation	p.Glu545Gly(p.E545G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58874226:58874226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2944G>A
AA Mutation	p.Glu982Lys(p.E982K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58874512:58874512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2757T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58872638:58872638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3294T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58882984:58882984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58874506:58874506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139969938
CDS Mutation	c.2763G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58880855:58880855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774290942
CDS Mutation	c.1527G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000320743
Start	58877485:58877485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2451C>A
AA Mutation	p.Cys817Ter(p.C817*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320743
Start	58877700:58877701(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2235dupT
AA Mutation	p.Ala746CysfsTer16(p.A746Cfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000320743
Start	58874331:58874332(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2840-2dupA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LRIG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58877658:58877658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2278A>T
AA Mutation	p.Ser760Cys(p.S760C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58914006:58914006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359C>T
AA Mutation	p.Ser120Leu(p.S120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58874182:58874182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2988G>T
AA Mutation	p.Lys996Asn(p.K996N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58888383:58888383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893C>A
AA Mutation	p.Ala298Asp(p.A298D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58874312:58874312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2858G>T
AA Mutation	p.Arg953Ile(p.R953I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58880698:58880698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684T>C
AA Mutation	p.Tyr562His(p.Y562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58874297:58874297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2873A>G
AA Mutation	p.Asp958Gly(p.D958G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58877632:58877632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2304G>T
AA Mutation	p.Glu768Asp(p.E768D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000320743
Start	58885886:58885886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Trp(p.R397W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320743
Start	58876461:58876461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2679A>G
Mutation Classification	Silent
Feature Type	Transcript