Colon Cancer: Gene >> LDLRAD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359446
Start	13645527:13645527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Asp(p.G264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359446
Start	13438364:13438364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Pro54Leu(p.P54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359446
Start	13645401:13645401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665C>T
AA Mutation	p.Ala222Val(p.A222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359446
Start	13645165:13645165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140766330
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359446
Start	13645351:13645351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359446
Start	13438263:13438263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LDLRAD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359446
Start	13645229:13645229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>A
AA Mutation	p.Glu165Lys(p.E165K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript