Colon Cancer: Gene >> NR2F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588126:93588126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Cys(p.R225C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327111
Start	93587917:93587917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464C>T
AA Mutation	p.Ala155Val(p.A155V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588022:93588022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569C>T
AA Mutation	p.Ser190Leu(p.S190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327111
Start	93585486:93585486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>A
AA Mutation	p.Ala155Thr(p.A155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93593682:93593682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112T>G
AA Mutation	p.Leu371Arg(p.L371R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588329:93588329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588386:93588386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93587966:93587966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93587996:93587996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93588146:93588146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327111
Start	93593782:93593782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761244180
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NR2F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93593768:93593768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198G>A
AA Mutation	p.Glu400Lys(p.E400K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588357:93588357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904T>G
AA Mutation	p.Phe302Val(p.F302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93585343:93585343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320A>C
AA Mutation	p.Lys107Thr(p.K107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327111
Start	93588037:93588037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584C>T
AA Mutation	p.Ala195Val(p.A195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript