Colon Cancer: Gene >> NR2F6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291442
Start	17235516:17235516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923T>A
AA Mutation	p.Ile308Asn(p.I308N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291442
Start	17245040:17245040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Asp61Asn(p.D61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000291442
Start	17232624:17232624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761684813
CDS Mutation	c.943G>A
AA Mutation	p.Ala315Thr(p.A315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291442
Start	17232465:17232465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102A>G
AA Mutation	p.Ile368Val(p.I368V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291442
Start	17245072:17245072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149C>A
AA Mutation	p.Pro50Gln(p.P50Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291442
Start	17235515:17235515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291442
Start	17232481:17232481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NR2F6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291442
Start	17232418:17232418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>T
AA Mutation	p.Glu383Asp(p.E383D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript