Colon Cancer: Gene >> NFIX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000592199
Start	13090331:13090331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435C>T
AA Mutation	p.Arg479Trp(p.R479W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000592199
Start	13073999:13073999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791G>A
AA Mutation	p.Arg264Gln(p.R264Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000592199
Start	13025513:13025513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786205515
CDS Mutation	c.520G>T
AA Mutation	p.Glu174Ter(p.E174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NFIX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000592199
Start	13025376:13025376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383G>A
AA Mutation	p.Arg128Gln(p.R128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000592199
Start	13075605:13075605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889G>A
AA Mutation	p.Gly297Arg(p.G297R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript