Colon Cancer: Gene >> ZNF281

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200409009:200409009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697G>A
AA Mutation	p.Ala233Thr(p.A233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200408067:200408067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639G>A
AA Mutation	p.Ala547Thr(p.A547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200409332:200409332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374T>G
AA Mutation	p.Val125Gly(p.V125G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200409606:200409606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Ser(p.G34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200407321:200407321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385A>C
AA Mutation	p.Lys795Asn(p.K795N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200408788:200408788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200409190:200409190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200408173:200408173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200408158:200408158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200407204:200407204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2502G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200408377:200408377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139544425
CDS Mutation	c.1329C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200407183:200407183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759164804
CDS Mutation	c.2523G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294740
Start	200409431:200409431(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.275delC
AA Mutation	p.Pro92LeufsTer7(p.P92Lfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294740
Start	200409199:200409199(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.507delG
AA Mutation	p.Ser170ValfsTer155(p.S170Vfs*155)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000294740
Start	200408763:200408763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943A>T
AA Mutation	p.Lys315Ter(p.K315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF281

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200407748:200407748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1958G>A
AA Mutation	p.Gly653Asp(p.G653D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200408089:200408089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1617G>T
AA Mutation	p.Lys539Asn(p.K539N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200408876:200408876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830G>A
AA Mutation	p.Arg277Gln(p.R277Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200408780:200408780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926A>T
AA Mutation	p.Lys309Ile(p.K309I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294740
Start	200408923:200408923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783T>G
AA Mutation	p.His261Gln(p.H261Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294740
Start	200407147:200407147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2559T>G
Mutation Classification	Silent
Feature Type	Transcript