Colon Cancer: Gene >> NR2F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96334532:96334532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899A>G
AA Mutation	p.Glu300Gly(p.E300G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96337540:96337540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163G>A
AA Mutation	p.Gly388Asp(p.G388D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96334303:96334303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670G>A
AA Mutation	p.Val224Ile(p.V224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96334150:96334150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517A>T
AA Mutation	p.Asn173Tyr(p.N173Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96337489:96337489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96334300:96334300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Ala223Thr(p.A223T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96337473:96337473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Cys(p.R366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394166
Start	96334544:96334544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911C>T
AA Mutation	p.Ala304Val(p.A304V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394166
Start	96334449:96334449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394166
Start	96334125:96334125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394166
Start	96332514:96332514(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.413delA
AA Mutation	p.Lys138SerfsTer7(p.K138Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NR2F2

No Mutation Annotation!