Colon Cancer: Gene >> NR6A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000487099
Start	124536033:124536033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924C>A
AA Mutation	p.Phe308Leu(p.F308L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000487099
Start	124554439:124554439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Trp(p.R92W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000487099
Start	124526814:124526814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166A>G
AA Mutation	p.Tyr389Cys(p.Y389C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000487099
Start	124538194:124538195(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.721dupC
AA Mutation	p.Gln241ProfsTer33(p.Q241Pfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NR6A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000487099
Start	124540170:124540170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538806855
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000487099
Start	124535937:124535937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020C>A
Mutation Classification	Silent
Feature Type	Transcript