Colon Cancer: Gene >> ZNF417

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57908845:57908845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433G>A
AA Mutation	p.Cys478Tyr(p.C478Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57909092:57909092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754090586
CDS Mutation	c.1186G>A
AA Mutation	p.Val396Ile(p.V396I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57908884:57908884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534115229
CDS Mutation	c.1394C>T
AA Mutation	p.Ala465Val(p.A465V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57908945:57908945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333T>A
AA Mutation	p.Phe445Ile(p.F445I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57909520:57909520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758T>C
AA Mutation	p.Val253Ala(p.V253A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57909847:57909847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431G>A
AA Mutation	p.Gly144Glu(p.G144E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312026
Start	57916402:57916402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10G>C
AA Mutation	p.Ala4Pro(p.A4P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312026
Start	57908574:57908574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312026
Start	57908641:57908642(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1636dupA
AA Mutation	p.Arg546LysfsTer4(p.R546Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF417

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312026
Start	57908952:57908952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1326G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000312026
Start	57908645:57908645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1633G>T
AA Mutation	p.Glu545Ter(p.E545*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript