Colon Cancer: Gene >> ZNF143

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396602
Start	9508795:9508795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324G>A
AA Mutation	p.Asp442Asn(p.D442N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396602
Start	9471376:9471376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762077968
CDS Mutation	c.68C>T
AA Mutation	p.Ala23Val(p.A23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396602
Start	9508705:9508705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1234A>G
AA Mutation	p.Thr412Ala(p.T412A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396602
Start	9512512:9512512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763052310
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396602
Start	9472756:9472756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753018534
CDS Mutation	c.192A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396602
Start	9516284:9516284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201816187
CDS Mutation	c.1608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000396602
Start	9494712:9494712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Ter(p.R238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF143

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396602
Start	9508780:9508780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309C>T
AA Mutation	p.Arg437Trp(p.R437W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396602
Start	9516209:9516209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533A>G
AA Mutation	p.Ile511Met(p.I511M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396602
Start	9497763:9497763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396602
Start	9501116:9501116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147334022
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000396602
Start	9474549:9474549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript