Colon Cancer: Gene >> ZBED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2489676:2489676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>G
AA Mutation	p.Ser348Arg(p.S348R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2489650:2489650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761629511
CDS Mutation	c.1070C>T
AA Mutation	p.Thr357Met(p.T357M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490443:2490443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490035:2490035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685G>T
AA Mutation	p.Gly229Cys(p.G229C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490386:2490386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774599670
CDS Mutation	c.334G>A
AA Mutation	p.Val112Ile(p.V112I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2489554:2489554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166G>A
AA Mutation	p.Ser389Asn(p.S389N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490659:2490659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747063221
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490566:2490566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Ala52Thr(p.A52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490077:2490077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764808495
CDS Mutation	c.643G>A
AA Mutation	p.Ala215Thr(p.A215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490125:2490125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595G>A
AA Mutation	p.Asp199Asn(p.D199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490449:2490449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775831950
CDS Mutation	c.271G>A
AA Mutation	p.Ala91Thr(p.A91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2488803:2488803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2489265:2489265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1455C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2490615:2490615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754614717
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2488782:2488782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1938T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2490153:2490153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145336488
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381218
Start	2489517:2489517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381218
Start	2490051:2490051(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.669delC
AA Mutation	p.Asn224ThrfsTer10(p.N224Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381218
Start	2490050:2490051(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.669dupC
AA Mutation	p.Asn224GlnfsTer30(p.N224Qfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381218
Start	2489103:2489104(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1616dupC
AA Mutation	p.Pro540AlafsTer80(p.P540Afs*80)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZBED1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2489027:2489027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693C>T
AA Mutation	p.His565Tyr(p.H565Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2490626:2490626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Asp32Asn(p.D32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381218
Start	2489654:2489654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066A>T
AA Mutation	p.Ser356Cys(p.S356C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript