Colon Cancer: Gene >> DZIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95589164:95589164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017T>C
AA Mutation	p.Ser673Pro(p.S673P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95624862:95624862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878A>G
AA Mutation	p.Glu293Gly(p.E293G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95630084:95630084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>T
AA Mutation	p.Leu239Phe(p.L239F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95587569:95587569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188G>A
AA Mutation	p.Glu730Lys(p.E730K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95587580:95587580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2177G>A
AA Mutation	p.Gly726Glu(p.G726E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95589197:95589197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1984A>C
AA Mutation	p.Asn662His(p.N662H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95611487:95611487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321G>T
AA Mutation	p.Asp441Tyr(p.D441Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95619931:95619931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127C>T
AA Mutation	p.Ala376Val(p.A376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95641650:95641650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576293914
CDS Mutation	c.242C>T
AA Mutation	p.Ala81Val(p.A81V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95587658:95587658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099C>T
AA Mutation	p.Pro700Leu(p.P700L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95584834:95584834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2426A>C
AA Mutation	p.Lys809Thr(p.K809T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95633309:95633309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610G>T
AA Mutation	p.Asp204Tyr(p.D204Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95587542:95587542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376315570
CDS Mutation	c.2215G>T
AA Mutation	p.Ala739Ser(p.A739S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95590358:95590358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1764A>G
AA Mutation	p.Ile588Met(p.I588M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95584906:95584906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138276983
CDS Mutation	c.2354C>T
AA Mutation	p.Ala785Val(p.A785V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95624786:95624786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138320927
CDS Mutation	c.954G>T
AA Mutation	p.Lys318Asn(p.K318N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95630090:95630090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95584749:95584749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2511G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95590286:95590286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95584848:95584848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200670080
CDS Mutation	c.2412A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95587570:95587570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780873105
CDS Mutation	c.2187C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347108
Start	95586027:95586027(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2328delA
AA Mutation	p.Glu777LysfsTer6(p.E777Kfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347108
Start	95584842:95584842(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2418delA
AA Mutation	p.Lys806AsnfsTer22(p.K806Nfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95582305:95582305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2533G>T
AA Mutation	p.Glu845Ter(p.E845*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95612153:95612153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Ter(p.R400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95599386:95599386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>T
AA Mutation	p.Glu506Ter(p.E506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DZIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95641299:95641299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593A>G
AA Mutation	p.Tyr198Cys(p.Y198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95609507:95609507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1370C>A
AA Mutation	p.Pro457His(p.P457H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347108
Start	95633295:95633295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624G>T
AA Mutation	p.Met208Ile(p.M208I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95594070:95594070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95587645:95587645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111764824
CDS Mutation	c.2112G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347108
Start	95630070:95630070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147346095
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95612153:95612153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Arg400Ter(p.R400*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95619896:95619896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162G>T
AA Mutation	p.Glu388Ter(p.E388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000347108
Start	95590339:95590339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756109756
CDS Mutation	c.1783C>T
AA Mutation	p.Arg595Ter(p.R595*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript