Colon Cancer: Gene >> ZFP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178931783:178931783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>A
AA Mutation	p.Pro157His(p.P157H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178931904:178931904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>T
AA Mutation	p.Lys197Asn(p.K197N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178931534:178931534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221A>G
AA Mutation	p.His74Arg(p.H74R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178932421:178932421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745927279
CDS Mutation	c.1108A>G
AA Mutation	p.Thr370Ala(p.T370A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178932694:178932694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381A>G
AA Mutation	p.Thr461Ala(p.T461A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178932182:178932182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139498546
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178932677:178932677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376015846
CDS Mutation	c.1364G>A
AA Mutation	p.Arg455Gln(p.R455Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178932117:178932117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804A>C
AA Mutation	p.Lys268Asn(p.K268N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361362
Start	178932168:178932168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361362
Start	178931868:178931868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000361362
Start	178932049:178932049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>T
AA Mutation	p.Glu246Ter(p.E246*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361362
Start	178931762:178931762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376749929
CDS Mutation	c.449G>T
AA Mutation	p.Arg150Ile(p.R150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript