Colon Cancer: Gene >> ZNF304

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356783:57356783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>T
AA Mutation	p.Arg305Ile(p.R305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57351675:57351675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11C>T
AA Mutation	p.Ala4Val(p.A4V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357188:57357188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319T>A
AA Mutation	p.Val440Asp(p.V440D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357211:57357211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146642030
CDS Mutation	c.1342G>A
AA Mutation	p.Val448Met(p.V448M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357119:57357119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250G>C
AA Mutation	p.Arg417Thr(p.R417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57353845:57353845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154A>G
AA Mutation	p.Thr52Ala(p.T52A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357743:57357743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753022221
CDS Mutation	c.1874G>A
AA Mutation	p.Ser625Asn(p.S625N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000282286
Start	57353727:57353727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36T>A
AA Mutation	p.Ser12Arg(p.S12R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356759:57356759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890A>G
AA Mutation	p.His297Arg(p.H297R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356989:57356989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Cys(p.R374C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357316:57357316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1447G>A
AA Mutation	p.Ala483Thr(p.A483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357248:57357248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1379A>T
AA Mutation	p.Asp460Val(p.D460V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357829:57357829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960G>T
AA Mutation	p.Ala654Ser(p.A654S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282286
Start	57357483:57357483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1614A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282286
Start	57356232:57356232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF304

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57351672:57351672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356852:57356852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983T>A
AA Mutation	p.Val328Asp(p.V328D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357112:57357112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759725667
CDS Mutation	c.1243G>A
AA Mutation	p.Gly415Arg(p.G415R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356663:57356663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794C>A
AA Mutation	p.Ala265Asp(p.A265D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57356989:57356989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Cys(p.R374C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282286
Start	57357579:57357579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1710T>A
AA Mutation	p.Ser570Arg(p.S570R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282286
Start	57356337:57356337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript