Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NR1I3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367982
Start	161235904:161235904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748184864
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367982
Start	161233218:161233218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359C>T
AA Mutation	p.Ala120Val(p.A120V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367982
Start	161233285:161233285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367982
Start	161231329:161231329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694G>T
AA Mutation	p.Val232Leu(p.V232L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant;coding_sequence_variant
Transcription ID	ENST00000367982
Start	161235846:161235849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.236_238+1delACAG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NR1I3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367982
Start	161235897:161235897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747474209
CDS Mutation	c.188G>A
AA Mutation	p.Cys63Tyr(p.C63Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367982
Start	161236492:161236492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756548242
CDS Mutation	c.74C>T
AA Mutation	p.Ala25Val(p.A25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367982
Start	161229863:161229863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367982
Start	161231127:161231127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813C>A
Mutation Classification	Silent
Feature Type	Transcript