Colon Cancer: Gene >> ZNF79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342483
Start	127444794:127444794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094C>T
AA Mutation	p.Ala365Val(p.A365V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342483
Start	127444716:127444716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016G>T
AA Mutation	p.Gly339Val(p.G339V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342483
Start	127445020:127445020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774122662
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342483
Start	127444735:127444735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373770489
CDS Mutation	c.1035C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342483
Start	127444106:127444106(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.410delC
AA Mutation	p.Pro137LeufsTer17(p.P137Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342483
Start	127444847:127444848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1150_1151delAC
AA Mutation	p.Thr384TrpfsTer34(p.T384Wfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000342483
Start	127435907:127435907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342483
Start	127444240:127444240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540G>T
AA Mutation	p.Lys180Asn(p.K180N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342483
Start	127444200:127444200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768639048
CDS Mutation	c.500C>T
AA Mutation	p.Ala167Val(p.A167V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript