Colon Cancer: Gene >> LGR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367278
Start	202318156:202318156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761460371
CDS Mutation	c.1853T>C
AA Mutation	p.Leu618Pro(p.L618P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367278
Start	202318465:202318465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77340941
CDS Mutation	c.2162C>T
AA Mutation	p.Ala721Val(p.A721V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367278
Start	202276388:202276388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Asp171Asn(p.D171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367278
Start	202310322:202310322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532C>A
AA Mutation	p.Pro511His(p.P511H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367278
Start	202318965:202318965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2662C>T
AA Mutation	p.Pro888Ser(p.P888S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202318199:202318199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540125583
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202310323:202310323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202307345:202307345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146190126
CDS Mutation	c.1224C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202276387:202276387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373499034
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202318463:202318463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3820385
CDS Mutation	c.2160C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202318121:202318121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769641205
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000367278
Start	202318037:202318037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1734C>A
AA Mutation	p.Cys578Ter(p.C578*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000367278
Start	202235986:202235986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421C>T
AA Mutation	p.Gln141Ter(p.Q141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000367278
Start	202310282:202310282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492G>T
AA Mutation	p.Glu498Ter(p.E498*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000367278
Start	202276522:202276522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LGR6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202318292:202318292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758170595
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367278
Start	202304565:202304565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367278
Start	202318078:202318078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs113146160
CDS Mutation	c.1775delT
AA Mutation	p.Val592AlafsTer10(p.V592Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript