Colon Cancer: Gene >> NR1I2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119810080:119810080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217G>A
AA Mutation	p.Ala73Thr(p.A73T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119810101:119810101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Trp(p.R80W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119807374:119807374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776219511
CDS Mutation	c.124C>T
AA Mutation	p.Arg42Cys(p.R42C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119807254:119807254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4G>A
AA Mutation	p.Glu2Lys(p.E2K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119815349:119815349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964C>T
AA Mutation	p.Pro322Ser(p.P322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393716
Start	119810075:119810075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212G>A
AA Mutation	p.Arg71His(p.R71H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393716
Start	119810079:119810079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773536011
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393716
Start	119810097:119810097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393716
Start	119812813:119812813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.652delG
AA Mutation	p.Glu218ArgfsTer59(p.E218Rfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NR1I2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393716
Start	119812730:119812730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564G>T
Mutation Classification	Silent
Feature Type	Transcript