Colon Cancer: Gene >> NR2E3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71811809:71811809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775720634
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71813500:71813500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764901119
CDS Mutation	c.859G>A
AA Mutation	p.Gly287Ser(p.G287S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71817610:71817610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>A
AA Mutation	p.Glu387Lys(p.E387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71812069:71812069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71810796:71810796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53C>A
AA Mutation	p.Pro18His(p.P18H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71813572:71813572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767442358
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Trp(p.R311W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617575
Start	71813499:71813499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617575
Start	71812436:71812436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530684859
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NR2E3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000617575
Start	71814015:71814015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554638593
CDS Mutation	c.998C>T
AA Mutation	p.Thr333Met(p.T333M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000617575
Start	71814016:71814016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772856819
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript