Colon Cancer: Gene >> ZNF582

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56384035:56384035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1382G>T
AA Mutation	p.Ser461Ile(p.S461I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301310
Start	56390094:56390094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>A
AA Mutation	p.Leu47Ile(p.L47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56384542:56384542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875T>G
AA Mutation	p.Phe292Cys(p.F292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301310
Start	56384181:56384181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000301310
Start	56384621:56384621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374319071
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Ter(p.R266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF582

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56384976:56384976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441A>C
AA Mutation	p.Glu147Asp(p.E147D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56384693:56384693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724T>G
AA Mutation	p.Phe242Val(p.F242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56390009:56390009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224T>A
AA Mutation	p.Leu75Gln(p.L75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56384341:56384341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777829187
CDS Mutation	c.1076G>T
AA Mutation	p.Arg359Ile(p.R359I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301310
Start	56390093:56390093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.140T>G
AA Mutation	p.Leu47Arg(p.L47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301310
Start	56384472:56384472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000301310
Start	56384133:56384133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1284T>A
AA Mutation	p.Cys428Ter(p.C428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript