Colon Cancer: Gene >> ZNF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614034
Start	95181649:95181649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377134231
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614034
Start	95177551:95177551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102A>G
AA Mutation	p.Ile34Met(p.I34M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614034
Start	95182081:95182081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756795227
CDS Mutation	c.1253G>A
AA Mutation	p.Arg418His(p.R418H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614034
Start	95181590:95181590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762G>T
AA Mutation	p.Glu254Asp(p.E254D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614034
Start	95181372:95181372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.549delT
AA Mutation	p.Phe183LeufsTer38(p.F183Lfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000614034
Start	95181797:95181798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.969_970delTG
AA Mutation	p.Tyr323Ter(p.Y323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614034
Start	95181140:95181141(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.318dupA
AA Mutation	p.Ser107IlefsTer18(p.S107Ifs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614034
Start	95181795:95181796(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.967_968insCC
AA Mutation	p.Tyr323SerfsTer7(p.Y323Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614034
Start	95181878:95181878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1050C>A
AA Mutation	p.Phe350Leu(p.F350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript