Colon Cancer: Gene >> ZBTB7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4054016:4054016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217G>T
AA Mutation	p.Gly406Val(p.G406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4054022:4054022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211A>G
AA Mutation	p.His404Arg(p.H404R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4054764:4054764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469G>A
AA Mutation	p.Ala157Thr(p.A157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4055205:4055205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28G>A
AA Mutation	p.Gly10Arg(p.G10R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4047943:4047943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756558497
CDS Mutation	c.1564G>A
AA Mutation	p.Ala522Thr(p.A522T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4047886:4047886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557211563
CDS Mutation	c.1621G>A
AA Mutation	p.Glu541Lys(p.E541K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322357
Start	4054013:4054013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220A>T
AA Mutation	p.Glu407Val(p.E407V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322357
Start	4055092:4055092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322357
Start	4054816:4054816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753160204
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322357
Start	4047854:4047854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1653C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000322357
Start	4054014:4054014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1219G>T
AA Mutation	p.Glu407Ter(p.E407*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000322357
Start	4053970:4053970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZBTB7A

No Mutation Annotation!