Colon Cancer: Gene >> ZFP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092966:5092966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763913364
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Trp(p.R488W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5091765:5091765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
AA Mutation	p.Glu87Asp(p.E87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092116:5092116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612G>T
AA Mutation	p.Lys204Asn(p.K204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092843:5092843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339A>G
AA Mutation	p.Lys447Glu(p.K447E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092322:5092322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818G>T
AA Mutation	p.Arg273Ile(p.R273I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5091929:5091929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Thr142Ile(p.T142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092808:5092808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304A>G
AA Mutation	p.Glu435Gly(p.E435G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5091893:5091893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389A>C
AA Mutation	p.Lys130Thr(p.K130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5091653:5091653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149A>G
AA Mutation	p.His50Arg(p.H50R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318833
Start	5091798:5091798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318833
Start	5092257:5092257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318833
Start	5092946:5092946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442A>C
AA Mutation	p.Glu481Ala(p.E481A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000318833
Start	5091937:5091937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>T
AA Mutation	p.Glu145Ter(p.E145*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript