Colon Cancer: Gene >> ZC3H12C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110165643:110165643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2558T>G
AA Mutation	p.Leu853Arg(p.L853R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110164847:110164847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768457807
CDS Mutation	c.1762G>A
AA Mutation	p.Gly588Arg(p.G588R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110165694:110165694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2609T>G
AA Mutation	p.Leu870Arg(p.L870R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110136880:110136880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764220083
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110136837:110136837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196C>A
AA Mutation	p.Pro66Thr(p.P66T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110164566:110164566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1481G>A
AA Mutation	p.Ser494Asn(p.S494N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110165094:110165094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2009G>A
AA Mutation	p.Arg670His(p.R670H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110137038:110137038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755763390
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Cys(p.R133C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110137300:110137300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370650723
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110164385:110164385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764161763
CDS Mutation	c.1300G>A
AA Mutation	p.Glu434Lys(p.E434K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110165699:110165699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543476423
CDS Mutation	c.2614G>A
AA Mutation	p.Ala872Thr(p.A872T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110137152:110137152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511A>G
AA Mutation	p.Lys171Glu(p.K171E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278590
Start	110136884:110136884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278590
Start	110164972:110164972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1887A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278590
Start	110165632:110165632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191947838
CDS Mutation	c.2547C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000278590
Start	110152932:110152932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787G>T
AA Mutation	p.Glu263Ter(p.E263*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZC3H12C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110164446:110164446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361C>T
AA Mutation	p.Thr454Met(p.T454M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110137263:110137263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Ala208Thr(p.A208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110164841:110164841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>A
AA Mutation	p.Asp586Asn(p.D586N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110165438:110165438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2353G>A
AA Mutation	p.Asp785Asn(p.D785N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278590
Start	110163336:110163336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>T
AA Mutation	p.Lys404Asn(p.K404N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278590
Start	110159305:110159305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764133995
CDS Mutation	c.963G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278590
Start	110164840:110164840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375663453
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript