Colon Cancer: Gene >> LRIG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66407466:66407466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769741661
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Trp(p.R321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66380823:66380823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749160433
CDS Mutation	c.2809G>A
AA Mutation	p.Glu937Lys(p.E937K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66380781:66380781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2851C>T
AA Mutation	p.Pro951Ser(p.P951S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66462441:66462441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>C
AA Mutation	p.Glu96Ala(p.E96A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66386254:66386254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516G>A
AA Mutation	p.Ala506Thr(p.A506T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66383336:66383336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2137C>A
AA Mutation	p.Gln713Lys(p.Q713K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66384182:66384182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1880A>G
AA Mutation	p.Asn627Ser(p.N627S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66384083:66384083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979C>T
AA Mutation	p.Thr660Ile(p.T660I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66384063:66384063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548930200
CDS Mutation	c.1999G>A
AA Mutation	p.Ala667Thr(p.A667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66451590:66451590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149854215
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66380375:66380375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3170T>A
AA Mutation	p.Val1057Asp(p.V1057D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66383261:66383261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200213153
CDS Mutation	c.2212C>T
AA Mutation	p.Arg738Trp(p.R738W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66380732:66380732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763466335
CDS Mutation	c.2900C>T
AA Mutation	p.Pro967Leu(p.P967L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273261
Start	66394062:66394063(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1445_1446delTG
AA Mutation	p.Val482AlafsTer9(p.V482Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273261
Start	66382276:66382286(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2604_2614delCATTGAGAGCA
AA Mutation	p.His868GlnfsTer44(p.H868Qfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000273261
Start	66382981:66382981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2491+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LRIG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66386127:66386127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1643T>G
AA Mutation	p.Val548Gly(p.V548G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273261
Start	66414948:66414948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Ala207Thr(p.A207T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66394047:66394047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66380713:66380713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2919G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273261
Start	66380398:66380398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138156364
CDS Mutation	c.3147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000273261
Start	66462442:66462442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>T
AA Mutation	p.Glu96Ter(p.E96*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript