Colon Cancer: Gene >> NR1H4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100563442:100563442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414G>T
AA Mutation	p.Asp472Tyr(p.D472Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100537020:100537020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934C>A
AA Mutation	p.Leu312Ile(p.L312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100563284:100563284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1256A>C
AA Mutation	p.Glu419Ala(p.E419A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100510967:100510967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113431969
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100510861:100510861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>A
AA Mutation	p.Pro65Thr(p.P65T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100536573:100536573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824A>G
AA Mutation	p.Asn275Ser(p.N275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100511021:100511021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353T>C
AA Mutation	p.Val118Ala(p.V118A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100532542:100532542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560G>T
AA Mutation	p.Arg187Ile(p.R187I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100536565:100536565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816T>G
AA Mutation	p.Asp272Glu(p.D272E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551379
Start	100511046:100511046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767379406
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551379
Start	100540775:100540775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569479207
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551379
Start	100510839:100510839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148156024
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000551379
Start	100540809:100540809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Ter(p.R367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NR1H4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551379
Start	100540810:100540810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762904675
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367Gln(p.R367Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551379
Start	100510950:100510950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000551379
Start	100536947:100536947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.862-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript