Colon Cancer: Gene >> LRP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53280697:53280697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386C>T
AA Mutation	p.Ala129Val(p.A129V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53275730:53275730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373908782
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53289634:53289634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779936452
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53280609:53280609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539938837
CDS Mutation	c.474G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53250741:53250741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2625A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53249392:53249392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2841C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53271309:53271309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53249404:53249404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764999429
CDS Mutation	c.2829C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53275647:53275647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990A>C
AA Mutation	p.Glu330Asp(p.E330D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53262193:53262193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789C>T
AA Mutation	p.Arg597Cys(p.R597C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53264196:53264196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628G>C
AA Mutation	p.Arg543Pro(p.R543P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306052
Start	53250809:53250809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2557C>T
AA Mutation	p.Arg853Trp(p.R853W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53264282:53264282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1542T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306052
Start	53271113:53271113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1167C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000306052
Start	53257464:53257465(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2210-1_2210insTT
AA Mutation	p.Ala737ValfsTer11(p.A737Vfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript