Colon Cancer: Gene >> ZNF518B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10443811:10443811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780296751
CDS Mutation	c.2518G>A
AA Mutation	p.Glu840Lys(p.E840K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444122:10444122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2207A>G
AA Mutation	p.Asn736Ser(p.N736S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444266:10444266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2063A>G
AA Mutation	p.His688Arg(p.H688R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10446088:10446088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241G>A
AA Mutation	p.Asp81Asn(p.D81N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444749:10444749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580T>C
AA Mutation	p.Leu527Ser(p.L527S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444053:10444053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2276G>A
AA Mutation	p.Arg759Lys(p.R759K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10443523:10443523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2806T>C
AA Mutation	p.Cys936Arg(p.C936R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10443124:10443124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3205C>A
AA Mutation	p.Leu1069Ile(p.L1069I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444469:10444469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1860T>G
AA Mutation	p.Asn620Lys(p.N620K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10445767:10445767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562T>C
AA Mutation	p.Phe188Leu(p.F188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444659:10444659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670G>T
AA Mutation	p.Ser557Ile(p.S557I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445492:10445492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10444034:10444034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2295T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10443446:10443446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201916292
CDS Mutation	c.2883G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445894:10445894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445290:10445290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766312027
CDS Mutation	c.1039T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445357:10445357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10443802:10443802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000326756
Start	10445908:10445908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421C>T
AA Mutation	p.Arg141Ter(p.R141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326756
Start	10445121:10445122(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1207dupA
AA Mutation	p.Thr403AsnfsTer7(p.T403Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF518B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10444411:10444411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918A>G
AA Mutation	p.Ser640Gly(p.S640G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10445686:10445686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643A>G
AA Mutation	p.Arg215Gly(p.R215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326756
Start	10443354:10443354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2975T>C
AA Mutation	p.Leu992Pro(p.L992P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445702:10445702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10445702:10445702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758696006
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326756
Start	10446056:10446056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141392062
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326756
Start	10445099:10445099(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1230delG
AA Mutation	p.Asn411MetfsTer6(p.N411Mfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript