Colon Cancer: Gene >> NR1H2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253727
Start	50378352:50378352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767999123
CDS Mutation	c.385G>A
AA Mutation	p.Gly129Arg(p.G129R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253727
Start	50382581:50382581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362G>T
AA Mutation	p.Glu454Asp(p.E454D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253727
Start	50379051:50379051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253727
Start	50377756:50377756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772224466
CDS Mutation	c.67G>A
AA Mutation	p.Ala23Thr(p.A23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253727
Start	50377623:50377623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375078500
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253727
Start	50382536:50382536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769755647
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253727
Start	50377755:50377755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544840857
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253727
Start	50378204:50378204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373402796
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253727
Start	50378279:50378279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373570078
CDS Mutation	c.312C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NR1H2

No Mutation Annotation!