Colon Cancer: Gene >> ZFP82

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393982:36393982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Asp120Tyr(p.D120Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393796:36393796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778648836
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Cys(p.R182C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36392764:36392764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576A>C
AA Mutation	p.Lys526Gln(p.K526Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393660:36393660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780307893
CDS Mutation	c.680A>T
AA Mutation	p.Glu227Val(p.E227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393498:36393498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842C>G
AA Mutation	p.Pro281Arg(p.P281R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36394065:36394065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275A>G
AA Mutation	p.Asp92Gly(p.D92G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393457:36393457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773772574
CDS Mutation	c.883G>A
AA Mutation	p.Ala295Thr(p.A295T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393452:36393452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888C>A
AA Mutation	p.His296Gln(p.H296Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393490:36393490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850T>G
AA Mutation	p.Cys284Gly(p.C284G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393423:36393423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917C>T
AA Mutation	p.Ala306Val(p.A306V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392161
Start	36393311:36393311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000392161
Start	36393341:36393342(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.990_998dupACTTCATAC
AA Mutation	p.Leu331_Thr333dup(p.L331_T333dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP82

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393976:36393976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>A
AA Mutation	p.Glu122Lys(p.E122K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36392917:36392917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>A
AA Mutation	p.Glu475Lys(p.E475K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36407976:36407976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47C>A
AA Mutation	p.Ser16Tyr(p.S16Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392161
Start	36393589:36393589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751G>A
AA Mutation	p.Glu251Lys(p.E251K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392161
Start	36393311:36393311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript